Публикации сотрудника подразделения БД НИОХ СО РАН

Монографии, главы в научных книгах, учебные пособия

2019

1. E.A. Pritchina, N.P. Gritsan, O.A. Rakitin, A.V. Zibarev
   2,1,3-Benzochalcogenadiazoles: regularities and peculiarities over a whole chalcogen pentad O, S, Se, Te and Po
   TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES, VOL 23 Серия книг: Targets in Heterocyclic Systems-Chemistry and Properties Targets in Heterocyclic Systems-Chemistry and Properties , 2019, 23, 143-154 doi:10.17374/targets.2020.23.143
2. E.A. Pritchina, N.P. Gritsan, O.A. Rakitin, A.V. Zibarev
   2,1,3-Benzochalcogenadiazoles: regularities and peculiarities over a whole chalcogen pentad O, S, Se, Te and Po
   TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES, VOL 23 Серия книг: Targets in Heterocyclic Systems-Chemistry and Properties Targets in Heterocyclic Systems-Chemistry and Properties , 2019, 23, 143-154 doi:10.17374/targets.2020.23.143
3. E.A. Pritchina, N.P. Gritsan, O.A. Rakitin, A.V. Zibarev
   2,1,3-Benzochalcogenadiazoles: regularities and peculiarities over a whole chalcogen pentad O, S, Se, Te and Po
   TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES, VOL 23 Серия книг: Targets in Heterocyclic Systems-Chemistry and Properties Targets in Heterocyclic Systems-Chemistry and Properties , 2019, 23, 143-154 doi:10.17374/targets.2020.23.143

2018

4. Э.Э. Шульц, В.Г. Карцев, Г.А. Толстиков
   Химия и биологическая активность индольных алкалоидов
   Издано по заказу Междунароного благотворителного фонда "Научное партнёрство", ООО "СОЛИД пресс", ISBN 970-5-903078-45-5, 2018, Усл. Печ. Л. 66, Тираж 250 экз.

2017

5. E. Karpova, G. Balakina, V. Vasiliev, V. Mamatyuk
   Determination of natural dyestuffs in historic textile with molecular spectroscopy and HPLC coupled with diode array and mass-selective detection
   In "The Diversity of Dyes in History and Archaeology" edited by Jo Kirby Atkinson, ISBN:9781909492530, Archetype Publications.London, 2017. P. 437-447.
6. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
   Наследие тибетской медицины в инновационных проектах Бурятии
   
7. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
   Наследие тибетской медицины в инновационных проектах Бурятии
   
8. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
   Наследие тибетской медицины в инновационных проектах Бурятии
   
9. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
   Наследие тибетской медицины в инновационных проектах Бурятии
   
10. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
    Наследие тибетской медицины в инновационных проектах Бурятии
    
11. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
    Наследие тибетской медицины в инновационных проектах Бурятии
    
12. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
    Наследие тибетской медицины в инновационных проектах Бурятии
    
13. Ю.Ж. Жабон, А.Г. Мондодоев, С.В. Морозов, М.П. Мошкин, Г.Г. Николаева, О.С. Ринчинов, Т.Г. Толстикова, Л.Н. Шантанова, В.М. Шишмарев, Т.М. Шишмарева
    Наследие тибетской медицины в инновационных проектах Бурятии
    
14. А.В. Ткачев, Д.Л. Прокушева, Д.В. Домрачев
    Дикорастущие эфирномасличные растения Южной Сибири. Атлас хроматографических профилей.
    ООО "Оффсет-ТМ", Новосибирск, 2017, Тираж 300 экз. печ. л. 32,5, ISBN 5978-5-85957-139-0

2016

15. O. Krumkacheva, E. Bagryanskaya
    Trityl radicals as spin labels
    From the book: Electron Paramagnetic Resonance: Volume 25, 2016, 25, 35-60. ISSN:978-1-78262-857-6 doi:10.1039/9781782629436-00035

2015

16. E. G. Bagryanskaya, O. A. Krumkacheva, M. V. Fedin, S. R. A. Marque
    Chapter Fourteen - Development and Application of Spin Traps, Spin Probes, and Spin Labels
    Methods in Enzymology, V. 563, 2015, Pp 365–396. Electron Paramagnetic Resonance Investigations of Biological Systems by Using Spin Labels, Spin Probes, and Intrinsic Metal Ions, Part A doi:10.1016/bs.mie.2015.06.004, IF=2.88
17. E. G. Bagryanskaya, O. A. Krumkacheva, M. V. Fedin, S. R. A. Marque
    Chapter Fourteen - Development and Application of Spin Traps, Spin Probes, and Spin Labels
    Methods in Enzymology, V. 563, 2015, Pp 365–396. Electron Paramagnetic Resonance Investigations of Biological Systems by Using Spin Labels, Spin Probes, and Intrinsic Metal Ions, Part A doi:10.1016/bs.mie.2015.06.004, IF=2.88

2014

18. K.P. Volcho, V.I. Anikeev
    Environmentally Benign Transformations of Monoterpenes and Monoterpenoids in Supercritical Fluids
    In: Anikeev V, Fan M, editors. Supercritical Fluid Technology for Energy and Environmental Applications. Elsevier; 2014. p. 69–87. ISBN: 9780444626967.
19. Шульц Э.Э., Карцев В.Г., Толстиков Г.A.
    Природные альфа-карболины. Синтез и биологическая активность
    в кн. "Химия гетероциклических соединений. Современные аспекты", М.: МБФНП, 2014, том 1, с. 521-538. (обзор)
20. Шульц Э.Э., Карцев В.Г., Толстиков Г.A.
    Синтез и биологическая активность природных гама-карболинов и их синтетических аналогов
    в кн. "Химия гетероциклических соединений. Современные аспекты", М.: МБФНП, 2014, том 1, с. 539-560. (обзор)
21. Шульц Э.Э., Карцев В.Г., Толстиков Г.A.
    Природные дельта-карболины. Синтез и биологическая активность
    в кн. "Химия гетероциклических соединений. Современные аспекты", М.: МБФНП, 2014, том 1, с. 561-575. (обзор)
22. Чернов Ю.В., Шульц Э.Э., Толстиков Г.А.
    Метиловый эфир 5-(2-{1-[2-(5-метокси-1H-индол-3-ил)-этил]-5-оксо-2,5-дигидро-1H-пиррол-3-ил}этил)-1,4а-диметил-6-метилендекагидронафталин-1-карбоновой кислоты
    в кн. "Химия гетероциклических соединений. Современные аспекты", М.: МБФНП, 2014, том 2, с. 579-580(избранные методики)
23. Василевский С.Ф., Михайловская Т. Ф.
    Новая анионная гетероциклизация-рециклизация гидразидов о-ацетиленилбензойных кислот.
    // В книге «Химия гетероциклических соединений. Современные аспекты. Том 1» под ред. В.Г.Карцева. – М.: «Научное партнерство, МБФНП, 2014 год, стр. 121 – 124.

2013

24. Л.Н. Рогоза, Н.Ф. Салахутдинов, С. Е. Толстиков, Г.А. Толстиков
    Препаративная химия терпеноидов: в 5 ч. Ч. 2(3). Смоляные кислоты – абиетиновая, дегидроабиетиновая, ламбертиановая, пимаровая, изопимаровая, левопимаровая
    Рос. Акад. наук, Сиб. отд-ние, Новосибирский институт органической химии. – Академиздат, 2013 – 316 с. ISBN 978-5-9904865-4-6.
25. Коковкин В.В., Шуваева О.В., Морозов С.В., Рапута В.Ф.
    Методическое пособие. Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации экспериментальных данных
    Новосибирск: НГУ, 2013. 82 с.
26. Коковкин В.В., Шуваева О.В., Морозов С.В., Рапута В.Ф.
    Методическое пособие. Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации экспериментальных данных
    Новосибирск: НГУ, 2013. 82 с.
27. Коковкин В.В., Шуваева О.В., Морозов С.В., Рапута В.Ф.
    Методическое пособие. Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации экспериментальных данных
    Новосибирск: НГУ, 2013. 82 с.
28. V.I. Ovcharenko, E.G. Bagryanskaya
    Breathing Crystals from Copper Nitroxyl Complexes
    In pin-Crossover Materials: Properties and Applications. Editor Malcolm A.Halcrow. John Wiley@ Sons, Ltd. Publication, 2013, – 564 p. ISBN: 978-1-119-99867-9 . DOI: 10.1002/9781118519301.ch9 http://eu.wiley.com/WileyCDA/WileyTitle/productCd-1119998670.html

2012

29. I. Boldov, N. Orlova, I. Kargapolova, A. Kuchyanov, V. Shelkovnikov, A. Plekhanov
    Optical Sensors Based on Opal Film and Silica Nanoparticles Modified with a Functional Dye.
    // in book: Advances in Chemical Sensors, Chapter 2, pp.29-46, Ed. by Wen Wang, InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5 InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5
30. I. Boldov, N. Orlova, I. Kargapolova, A. Kuchyanov, V. Shelkovnikov, A. Plekhanov
    Optical Sensors Based on Opal Film and Silica Nanoparticles Modified with a Functional Dye.
    // in book: Advances in Chemical Sensors, Chapter 2, pp.29-46, Ed. by Wen Wang, InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5 InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5
31. I. Boldov, N. Orlova, I. Kargapolova, A. Kuchyanov, V. Shelkovnikov, A. Plekhanov
    Optical Sensors Based on Opal Film and Silica Nanoparticles Modified with a Functional Dye.
    // in book: Advances in Chemical Sensors, Chapter 2, pp.29-46, Ed. by Wen Wang, InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5 InTech, - 2012 – 358 pp., ISBN 978-953-307-792-5
32. В.В. Коковкин, О.В. Шуваева, С.В. Морозов, В.Ф. Рапута
    Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации данных химического анализа
    Редакционно-издательский центр НГУ, Новосибирск, 85 стр.
33. В.В. Коковкин, О.В. Шуваева, С.В. Морозов, В.Ф. Рапута
    Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации данных химического анализа
    Редакционно-издательский центр НГУ, Новосибирск, 85 стр.
34. В.В. Коковкин, О.В. Шуваева, С.В. Морозов, В.Ф. Рапута
    Руководство по методам полевых и лабораторных исследований снежного покрова, численной интерпретации данных химического анализа
    Редакционно-издательский центр НГУ, Новосибирск, 85 стр.
35. V. V. Shelkovnikov, A.I. Plekhanov
    Optical and Resonant Non-Linear Optical Properties of J-Aggregates of Pseudoisocyanine Derivatives in Thin Solid Films
    // in book: “Macro To Nano Spectroscopy", Chapter 16, pp. 317-356., Ed. by Jamal Uddin, InTech, - 2012 – 448 pp. ISBN 978-953-51-0664-7 InTech, - 2012 – 448 pp. ISBN 978-953-51-0664-7
36. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, А.Г. Толстиков, Г.А. Толстиков
    «Монотерпеноиды в химии оптически активных феромонов насекомых»
    Рос. акад. наук, АИЦ «Наука», Москва, 2012. – 171 с., ISBN 978-5-02-037995-4
37. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, А.Г. Толстиков, Г.А. Толстиков
    «Монотерпеноиды в химии оптически активных феромонов насекомых»
    Рос. акад. наук, АИЦ «Наука», Москва, 2012. – 171 с., ISBN 978-5-02-037995-4
38. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, А.Г. Толстиков, Г.А. Толстиков
    «Монотерпеноиды в химии оптически активных феромонов насекомых»
    Рос. акад. наук, АИЦ «Наука», Москва, 2012. – 171 с., ISBN 978-5-02-037995-4
39. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, А.Г. Толстиков, Г.А. Толстиков
    «Монотерпеноиды в химии оптически активных феромонов насекомых»
    Рос. акад. наук, АИЦ «Наука», Москва, 2012. – 171 с., ISBN 978-5-02-037995-4
40. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
41. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
42. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
43. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
44. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
45. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
46. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
47. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
48. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
49. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
50. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
51. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
52. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
53. П.Е. Твердохлеб, В.В. Шелковников, Г.М. Жаркова, Ю.А. Щепеткин, Е.Ф. Пен, И.Ш. Штейнберг, М.Ю. Родионов, А.В. Трубецкой, Е.В. Васильев, В.А. Лоскутов, В.В. Русских, А.П. Петров, В.М. Хачатурян, А.Ю. Беликов, Н.Н. Вьюхина, В.Н. Затолокин, Д.Н. Иванов, И.Г. Шаталов
    Трехмерная лазерная модификация объемных светочувствительных материалов.
    Издательство СО РАН, 2012, ISBN 978-5-7692-1245-1, 350 стр. (35 усл. печ. л.)
54. A.V.Dushkin, T.G. Tolstikova, M.V.Khvostov, G. A. Tolstikov
    Complexes of Рolysaccharides and glycyrrhizin acid with drugs molecules. Mechanochemical synthesis and pharmacological
    // in book:“The Complex World of Polysaccharides”, ed.by Dr. D.N. Karunaratn., 648 p, Chapter 22, pp. 573-602. InTech, - 2012 – 634 pp , ISBN 978-953-51-0819-1
55. S.V. Vosel, A.A. Onischuk, P.A. Purtov, T.G. Tolstikova
    Classical nucleation theory: Account of dependence of the surface tension on curvature and translation-rotation correction factor
    //in book: “Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 19, pp. 503 – 528. CRC Press Taylor&Francis group London New York, 2012CRC Press Taylor&Francis group London New York, 2012
56. S.V. Vosel, A.A. Onischuk, P.A. Purtov, T.G. Tolstikova
    Classical nucleation theory: Account of dependence of the surface tension on curvature and translation-rotation correction factor
    //in book: “Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 19, pp. 503 – 528. CRC Press Taylor&Francis group London New York, 2012CRC Press Taylor&Francis group London New York, 2012
57. S.V. Vosel, A.A. Onischuk, P.A. Purtov, T.G. Tolstikova
    Classical nucleation theory: Account of dependence of the surface tension on curvature and translation-rotation correction factor
    //in book: “Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 19, pp. 503 – 528. CRC Press Taylor&Francis group London New York, 2012CRC Press Taylor&Francis group London New York, 2012
58. T.G . Tolstikova, A.A. Onischuk, I.V. Sorokina, A.M. Baklanov, V.V. Karasev, Boldyrev V.V., Fomin V.M.,M.V. Khvostov, A.O. Bryzgalov, G.A. Tolstikov
    Research and development of a new safe form of drug.
    //in book:“Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 11, PP 249-285, CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5
59. T.G . Tolstikova, A.A. Onischuk, I.V. Sorokina, A.M. Baklanov, V.V. Karasev, Boldyrev V.V., Fomin V.M.,M.V. Khvostov, A.O. Bryzgalov, G.A. Tolstikov
    Research and development of a new safe form of drug.
    //in book:“Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 11, PP 249-285, CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5
60. T.G . Tolstikova, A.A. Onischuk, I.V. Sorokina, A.M. Baklanov, V.V. Karasev, Boldyrev V.V., Fomin V.M.,M.V. Khvostov, A.O. Bryzgalov, G.A. Tolstikov
    Research and development of a new safe form of drug.
    //in book:“Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 11, PP 249-285, CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5
61. T.G . Tolstikova, A.A. Onischuk, I.V. Sorokina, A.M. Baklanov, V.V. Karasev, Boldyrev V.V., Fomin V.M.,M.V. Khvostov, A.O. Bryzgalov, G.A. Tolstikov
    Research and development of a new safe form of drug.
    //in book:“Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 11, PP 249-285, CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5
62. T.G . Tolstikova, A.A. Onischuk, I.V. Sorokina, A.M. Baklanov, V.V. Karasev, Boldyrev V.V., Fomin V.M.,M.V. Khvostov, A.O. Bryzgalov, G.A. Tolstikov
    Research and development of a new safe form of drug.
    //in book:“Aerosols Handbook, Measurement, Dosimetry and Health effects”, Ed. Ruser L.S. and Harley N. H., 648 p, Chapter 11, PP 249-285, CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5CRC Press Taylor&Francis group, London-New York - 2012 – 648 pp, ISBN 978-1-4398-5519-5

2011

63. О.А. Рабина, С.В. Морозов, Е.Н. Степанова
    Разработка и исследование стабильности к окислению функциональных продуктов на основе растительных и эфирных масел
    Современное состояние и перспективы развития пищевой промышленности и общественного питания: материалы V Международной научно-практической конференции, Т.1, С.40-43,Издательский центр ЮУрГУ, 2011, IBSN 978-5-696-04155-1
64. И.В. Зибарева, А.В. Зибарев, В.М. Бузник
    Библиометрический анализ российских химических исследований начала XXI века
    Науковедческие исследования. Сборник научных трудов (Отв. ред. Ракитов А.И.),РАН. ИНИОН. Центр научн,С. 127-154
65. В.Ф. Рапута, В.В. Коковкин, С.В.Морозов
    Модели и методы мониторинга загрязнения окрестностей автомагистралей. Раздел 1.7.
    //В кн. Геоинформационные технологии и математические модели для мониторинга и управления экологическими и социально-экономическими системами, Раздел 1.7., стр. 68-73,: Под. ред. Ю.И. Шокина и др.], Рос. акад. наук, Сиб. Отд., Ин-т водных и экологич. проблем, Барнаул:Пять плюс, - 2011 – 250 стр., ISBN 978-5-904014-23-0
66. В.Ф. Рапута, В.В. Коковкин, С.В.Морозов
    Модели и методы мониторинга загрязнения окрестностей автомагистралей. Раздел 1.7.
    //В кн. Геоинформационные технологии и математические модели для мониторинга и управления экологическими и социально-экономическими системами, Раздел 1.7., стр. 68-73,: Под. ред. Ю.И. Шокина и др.], Рос. акад. наук, Сиб. Отд., Ин-т водных и экологич. проблем, Барнаул:Пять плюс, - 2011 – 250 стр., ISBN 978-5-904014-23-0
67. В.А. Резников, А.Я. Тихонов, Т.Д. Федотова
    Химия в НГУ. Органическая химия для студентов
    Новосибирский государственный университет, 195 с
68. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
69. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
70. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
71. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
72. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
73. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
74. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
75. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
76. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
77. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
78. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
79. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
80. А.Н. Романов, В.Ф. Рапута, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, С.В. Морозов, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев
    Полиароматические углеводороды в пробах снежного покрова на территории ОАО «Алтай-Кокс»
    Материалы Российской научно-практической конф. «Инновации в онкологической практике».,Барнаул: АЗБУКА 2011 ,С. 362-365
81. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
82. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
83. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
84. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
85. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
86. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
87. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
88. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
89. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
90. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
91. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
92. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
93. С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова, В.А. Лубенников, А.Ф. Лазарев, А.Н. Романов, В.Ф. Рапута
    Оценка атмосферного загрязнения окружающей среды канцерогенными полиароматическими углеводородами по результатам химического анализа проб снегового покрова г. Барнаула
    Инновации в онкологической практике. 65 лет онкологической службе Алтайского края: Материалы Российской научно-практической конференции с международным участием 14-15 июля 2011 года г. Барнаул, Барнаул: Азбука, 2011,С. 359-362
94. A.V. Zibarev, R. Mews
    A new class of paramagnetics: 1,2,5-chalcogenadiazolidyl salts as potential building blocks for molecular magnets and conductors
    //Chapter 6 (pp.123-150) in book: Selenium and Tellurium Chemistry/Eds. J.D. Woollins, R.S. Laitinen. Springer - 2011. – 350 pp. ISBN 978-5-248-00514-7 Springer, 2011
95. Т.П. Кукина, Г.Г. Полякова, Н.В. Пашенова, Т.С. Фролова, И.К. Шундрина, О.И. Сальникова
    Изучение иммунной реакции сосны на заражение офиостомовыми грибами с помощью ХМС и ТГ/ДСК-анализа
    «Актуальные проблемы естественных наук»Новосибирск: Изд. «Априори» 2011, С.111-117
96. Т.П. Кукина, Г.Г. Полякова, Н.В. Пашенова, Т.С. Фролова, И.К. Шундрина, О.И. Сальникова
    Изучение иммунной реакции сосны на заражение офиостомовыми грибами с помощью ХМС и ТГ/ДСК-анализа
    «Актуальные проблемы естественных наук»Новосибирск: Изд. «Априори» 2011, С.111-117
97. Т.П. Кукина, О.И. Синицина, Т.С. Фролова
    Анализ генотоксических и антимутагенных свойств тритерпеноидов иван-чая узколистного
    «Проблемы современной науки: сборник научных трудов»Ставрополь: Центр научного знания «Логос», 2011
98. Т.П. Кукина, Е.В. Байкова
    Содержание урсоловой и олеаноловой кислот в некоторых видах шалфея
    Ставрополь: Центр научного знания «Логос», 2011, С. 17-24 (8 стр.) 0.500 у.п.л.
99. Г.А. Толстиков, Т.Г. Толстикова, Э.Э. Шульц, С.Е. Толстиков, М.В. Хвостов.
    Смоляные кислоты хвойных России. Химия, фармакология
    Академические издательство ГЕО. 2011 г. 395 c., ISBN 978-5-904682-67-5., уч.-изд. л. 33.1; уч.-печ. л. 34.7.
100. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
101. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
102. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
103. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
104. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
105. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281
106. И.Г. Боярских, А.И. Сысо, С.А. Худяев, С.П. Колотухин, А.И. Бакиянов, А.В. Шитов, В.Г. Васильев, О.В. Чанкина
     Реакция растений на изменения геофизических и почвенно-геохимических показателей среды в локальных геоактивных зонах горного Алтая (в монографии: Система «Планета Земля)»:
     //Глава (С. 262-281) в книге:Система «Планета Земля»: Русский путь:Рублев-Ломоносов-Гагарин /под ред. Федорова А.Е. – М.; ЛЕНАНД, 2011. - 514 стр. ISBN: 978-5-9710-0408-0. http://urss.ru/cgi-bin/db.pl?lang=Ru&blang=ru&page=Book&id=127136–М.; ЛЕНАНД, 2011, сс. 262-281

2010

107. Т.Г. Толстикова, А.Г. Толстиков, Г.А. Толстиков
     Лекарства из растительных веществ
     «ГЕО», Новосибирск, 2010, ISBN 978-5-904682-25-5
108. Бузник В.М., Зибарева И.В.
     Библиометрический анализ научной деятельности академика Ю. А. Буслаева
     Академик Юрий Александрович Буслаев / Под ред. акад. В. М. Бузника. М.: Интерконтакт Наука, 2009. С. 36–46 (11 стр.; всего – 46 стр.; 2.2 печ. л.).М.: Интерконтакт Наука, 2009
109. Зибарева И.В., Бузник В.М.
     Chemical Abstracts: база данных для библиометрических исследований
     Наука России. От настоящего к будущему / Ред. В. С. Арутюнов, Г. В. Лисичкин, Г. Г. Малинецкий. М: Либроком, 2009. С. 477–488 (12 стр.; всего – 512 стр.; 32 печ. л.).Либроком, 2009

2009

110. Н. А. Панкрушина, И.А. Никитина, Е.И. Черняк, С.А. Мызь, Т.П. Шахтшнейдер, В.В. Болдырев
     Механохимический синтез производных природного алкалоида лаппаконитина и синтетического лекарственного средства пироксикама
     В книге: «Фундаментальные основы механической активации, синтеза и механических технологий», глава 3. Вопросы теории и применения механохимического синтеза неорганических и органических соединений. Ред. Е.Г. Аввакумов, Издательство СО РАН, Новосибирск, 2009, С. 228-235
111. Н. А. Панкрушина, И.А. Никитина, Е.И. Черняк, С.А. Мызь, Т.П. Шахтшнейдер, В.В. Болдырев
     Механохимический синтез производных природного алкалоида лаппаконитина и синтетического лекарственного средства пироксикама
     В книге: «Фундаментальные основы механической активации, синтеза и механических технологий», глава 3. Вопросы теории и применения механохимического синтеза неорганических и органических соединений. Ред. Е.Г. Аввакумов, Издательство СО РАН, Новосибирск, 2009, С. 228-235
112. Н. А. Панкрушина, И.А. Никитина, Е.И. Черняк, С.А. Мызь, Т.П. Шахтшнейдер, В.В. Болдырев
     Механохимический синтез производных природного алкалоида лаппаконитина и синтетического лекарственного средства пироксикама
     В книге: «Фундаментальные основы механической активации, синтеза и механических технологий», глава 3. Вопросы теории и применения механохимического синтеза неорганических и органических соединений. Ред. Е.Г. Аввакумов, Издательство СО РАН, Новосибирск, 2009, С. 228-235
113. А.Я. Тихонов, Л.Б. Володарский
     Азотистые гетероциклы на основе 1,2- и 1,3-гидроксиламинооксимов
     Химия ароматических, гетероциклических и природных соединений Новосибирск: ЗAO ИПП “Офсет”. 2009
114. Лушникова Е.Л., Непомнящих Л.М., Толстикова Т.Г., печ. Л. 17
     Патоморфология мышечных клеток сердца при действии циклофосфамида и тритерпеноидов
     Москва, Издательство РАМН, отпечатано в ООО «Издательский дом «Вояж», Новосибирск, 2009. – 271 с. – 17.0 уч.-изд. л. ISBN-978-5-7901-0078-9.
115. Лушникова Е.Л., Непомнящих Л.М., Толстикова Т.Г., печ. Л. 17
     Патоморфология мышечных клеток сердца при действии циклофосфамида и тритерпеноидов
     Москва, Издательство РАМН, отпечатано в ООО «Издательский дом «Вояж», Новосибирск, 2009. – 271 с. – 17.0 уч.-изд. л. ISBN-978-5-7901-0078-9.
116. В.В. Шелковников, Е.В. Васильев, В.В. Русских, З.М. Иванова, Е.Ф. Пен, А.И. Плеханов, В.И. Ковалевский, И.А. Кучин, Е.В. Спесивцев, С.В. Рыхлицкий
     «Органические фотоактивные материалы для формирования и функционирования фотонных кристаллов» (объем 30 стр.),
     Глава в монографии «Фотонные кристаллы и нанокомпозиты: структурообразование, оптические и диэлектрические свойства» Ответственные редакторы: академик Шабанов В.Ф., ф.-м.н. Зырянов В.Я. ISBN 978-5-76-92-1096-9 (кн), 978-5-76-92-0669-6 печ.л. 21б печ.л. Гл. 1,3
117. В.В. Шелковников, Е.В. Васильев, В.В. Русских, З.М. Иванова, Е.Ф. Пен, А.И. Плеханов, В.И. Ковалевский, И.А. Кучин, Е.В. Спесивцев, С.В. Рыхлицкий
     «Органические фотоактивные материалы для формирования и функционирования фотонных кристаллов» (объем 30 стр.),
     Глава в монографии «Фотонные кристаллы и нанокомпозиты: структурообразование, оптические и диэлектрические свойства» Ответственные редакторы: академик Шабанов В.Ф., ф.-м.н. Зырянов В.Я. ISBN 978-5-76-92-1096-9 (кн), 978-5-76-92-0669-6 печ.л. 21б печ.л. Гл. 1,3
118. В.В. Шелковников, Е.В. Васильев, В.В. Русских, З.М. Иванова, Е.Ф. Пен, А.И. Плеханов, В.И. Ковалевский, И.А. Кучин, Е.В. Спесивцев, С.В. Рыхлицкий
     «Органические фотоактивные материалы для формирования и функционирования фотонных кристаллов» (объем 30 стр.),
     Глава в монографии «Фотонные кристаллы и нанокомпозиты: структурообразование, оптические и диэлектрические свойства» Ответственные редакторы: академик Шабанов В.Ф., ф.-м.н. Зырянов В.Я. ISBN 978-5-76-92-1096-9 (кн), 978-5-76-92-0669-6 печ.л. 21б печ.л. Гл. 1,3
119. В.В. Шелковников, Е.В. Васильев, В.В. Русских, З.М. Иванова, Е.Ф. Пен, А.И. Плеханов, В.И. Ковалевский, И.А. Кучин, Е.В. Спесивцев, С.В. Рыхлицкий
     «Органические фотоактивные материалы для формирования и функционирования фотонных кристаллов» (объем 30 стр.),
     Глава в монографии «Фотонные кристаллы и нанокомпозиты: структурообразование, оптические и диэлектрические свойства» Ответственные редакторы: академик Шабанов В.Ф., ф.-м.н. Зырянов В.Я. ISBN 978-5-76-92-1096-9 (кн), 978-5-76-92-0669-6 печ.л. 21б печ.л. Гл. 1,3
120. В.В. Шелковников, Е.В. Васильев, В.В. Русских, З.М. Иванова, Е.Ф. Пен, А.И. Плеханов, В.И. Ковалевский, И.А. Кучин, Е.В. Спесивцев, С.В. Рыхлицкий
     «Органические фотоактивные материалы для формирования и функционирования фотонных кристаллов» (объем 30 стр.),
     Глава в монографии «Фотонные кристаллы и нанокомпозиты: структурообразование, оптические и диэлектрические свойства» Ответственные редакторы: академик Шабанов В.Ф., ф.-м.н. Зырянов В.Я. ISBN 978-5-76-92-1096-9 (кн), 978-5-76-92-0669-6 печ.л. 21б печ.л. Гл. 1,3
121. Толстиков Г. А., Джемилев У. М., Толстиков А. Г.
     «Алюминийорганические соединения в органическом синтезе»
     Новосибирск, Акад. изд. «Гео», 2009. – 645 с. –уч.-изд. л. (Монография). ISBN-978-5-9747-0147-4.
122. Толстиков Г. А., Джемилев У. М., Толстиков А. Г.
     «Алюминийорганические соединения в органическом синтезе»
     Новосибирск, Акад. изд. «Гео», 2009. – 645 с. –уч.-изд. л. (Монография). ISBN-978-5-9747-0147-4.
123. Катраков И.Б., Карпова Е.В.
     Спектроскопические методы исследования органических соединений
     6.7 усл. печ. Листа,для студентов-химиков, изучающих специальный курс Спектроскопические методы исследования органических соединений,Барнаул: Изд-во Алтайского гос. ун-та, 2009. - 86 с
124. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
125. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
126. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
127. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
128. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
129. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
130. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
131. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
132. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
133. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
134. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
135. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
136. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
137. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
138. Н.Н. Булгаков, Е.И. Вовк, В.А. Иванченко, П.Н. Калинкин, А.Н. Кузьмин, А.А. Лысова, В.Н. Пармон, Е.В. Пархомчук, Д.И. Потапенко, В.А. Рогов, Е.Н. Савинов, В.А. Садыков, В.М. Тормышев, А.А. Хасин, А.П. Чупахин, А.А. Шубин
     Задачи по химической термодинамике
     Новосибирск, изд-во НГУ, 2009. Объем 6,2 усл.печ. Листов
139. В.Ф. Рапута, С.Е. Олькин, В.В. Коковкин, С.В. Морозов
     Экспериментальные исследования атмосферных выносов загрязняющих примесей с территории Новосибирска
     Государственный доклад «Состояние окружающей среды Новосибирской области в 2009 г.» Новосибирск, Департамент природных ресурсов и охраны окружающей среды Новосибирской области 2010, С. 13-17
140. В.Ф. Рапута, С.Е. Олькин, В.В. Коковкин, С.В. Морозов
     Экспериментальные исследования атмосферных выносов загрязняющих примесей с территории Новосибирска
     Государственный доклад «Состояние окружающей среды Новосибирской области в 2009 г.» Новосибирск, Департамент природных ресурсов и охраны окружающей среды Новосибирской области 2010, С. 13-17
141. В.Ф. Рапута, С.Е. Олькин, В.В. Коковкин, С.В. Морозов
     Экспериментальные исследования атмосферных выносов загрязняющих примесей с территории Новосибирска
     Государственный доклад «Состояние окружающей среды Новосибирской области в 2009 г.» Новосибирск, Департамент природных ресурсов и охраны окружающей среды Новосибирской области 2010, С. 13-17

2008

142. В.Л. Саленко, А.В. Шпатов
     Задачи и упражнения по органической химии. Индивидуальные задания для студентов.
     Новосибирский государственный архитектурно-строительный университет (Сибстрин), 25 стр., 100 экз.
143. И.А. Григорьев, И.Г. Иртегова, Е.Ш. Каган, И.Ю. Жукова
     Электрохимия нитроксильных радикалов
     Глава 7 в кн. «Электрохимия органических соединений в начале XXI века». 2008 г., Москва, изд-во «Спутник», с. 315-377.
144. И.А. Григорьев, И.Г. Иртегова, Е.Ш. Каган, И.Ю. Жукова
     Электрохимия нитроксильных радикалов
     Глава 7 в кн. «Электрохимия органических соединений в начале XXI века». 2008 г., Москва, изд-во «Спутник», с. 315-377.
145. Т.Н. Черемисина, А.В. Шпатов
     Химическая термодинамика. Методические указания по выполнению лабораторных работ для студентов I курса.
     Новосибирский государственный архи¬тектурно-строительный университет (Сибстрин), 30 стр., 100 экз.

2007

146. I.A. Grigor’ev, Nitrones
     Novel Strategies in Synthesis
     //In Book: Nitrile Oxides, Nitrones and Nitronates in Organic Synthesis: Novel Strategies in Synthesis, Second edition (ed. H.Feuer), John Wiley@Sons, Inc., 2007, Ch.2, pp.129-434
147. H.-J. Frohn, V.V. Bardin
     Organoxenonium salts. Synthesis by "xenodeborylation", reactivities, and NMR spectroscopic properties
     Recent Developments in Carbocation and Onium Ion Chemistry. ACS Symposium Series 965. K.K. Laali (Ed.) Oxford University Press, 2007
148. В.М. Бузник, И.В. Зибарева, Л.С. Филатова
     «Наукометрические показатели академика Ю.А. Золотова (по материалам баз данных Chemical Abstracts и Science Citation Index)»
     //В книге: "Успехи аналитической химии: к 75-летию академика Ю.А. Золотова " /[отв. ред. Л.К. Шпигун]; Ин-т общей и неорганической химии им. Н.С. Курнакова РАН. – М.: Наука, 2007. – с. 40-51.
149. Г.А. Толстиков, Л.А. Балтина, В.П. Гранкина, Р.М. Кондратенко, Т.Г. Толстикова
     «Солодка. Биоразнообразие, химия, применение в медицине»
     Новосибирск. Академическое изд. «ГЕО» 2007. с.238.
150. Г.А. Толстиков, Л.А. Балтина, В.П. Гранкина, Р.М. Кондратенко, Т.Г. Толстикова
     «Солодка. Биоразнообразие, химия, применение в медицине»
     Новосибирск. Академическое изд. «ГЕО» 2007. с.238.
151. Г.А. Толстиков, Л.А. Балтина, В.П. Гранкина, Р.М. Кондратенко, Т.Г. Толстикова
     «Солодка. Биоразнообразие, химия, применение в медицине»
     Новосибирск. Академическое изд. «ГЕО» 2007. с.238.

2006

152. Фурин Г.Г., Юматов В.Д.
     «Новое в химии полифторароматических соединений
     Новосибирск: Изд-во НГПУ, 2006, 25,6 уч. изд.л., 218 стр., 200 экз.
153. E.E. Shults, G.A. Tolstikov, V.G. Kartsev
     "Natural beta-carbolines: Synthesis and biological activity"
     in "Selected methods for synthesis and modification of heterocycles: Carbolines: Chemistry andbiological activity", Kartsev V.G., Ed., Moscow: Published by the International Charitable Scientific Partnership Foundation (ICSPF), 2006, vol. 5, p. 153-299
154. E.E. Shults, G.A. Tolstikov, V.G. Kartsev
     "Naturally occurring alfa-, gamma-, delta-carbolines and their analogs: Synthesis and biological activity"
     in "Selected methods for synthesis and modification of heterocycles: Carbolines: Chemistry and biological activity", Kartsev V.G., Ed., Moscow: Published by the International Charitable Scientific Partnership Foundation (ICSPF), 2006, vol. 5, p. 77-152.
155. А.В. Шпатов, В.Л. Саленко
     Индивидуальные задания "Органическая химия. Углеводороды" (для студентов III курса)
     Новосибирск, изд-во НГАСУ, 2006, 12 с., 50 экз.
156. В.А. Резников, Л.А. Осташевская, А.М. Чибиряев, А.Я. Тихонов, В.Н. Бережная, К.Ю. Колтунов
     Органическая химия. Модульная программа лекционного курса, семинаров, практикума и самостоятельной работы студентов (Курс 2-й, семестр III). Методическое пособие для студентов факультета естественных наук и медицинского факультета
     Новосибирск, РИЦ НГУ, 2006, 66 с., 100 экз.
157. В.А. Резников, Л.А. Осташевская, А.М. Чибиряев, А.Я. Тихонов, В.Н. Бережная, К.Ю. Колтунов
     Органическая химия. Модульная программа лекционного курса, семинаров, практикума и самостоятельной работы студентов (Курс 2-й, семестр III). Методическое пособие для студентов факультета естественных наук и медицинского факультета
     Новосибирск, РИЦ НГУ, 2006, 66 с., 100 экз.
158. L.I. Kurteeva, S.V. Morozov, A.G. Anshits
     Sources of carcinogenic PAH emission in aluminum production using Soderberg cell.
     // In: Advances in the Geological Storage of Carbon Dioxide, 2006, P. 57-65. // Eds. S. Lombardi, L.K. Altunina, S.E. Beaubien. NATO Science Series: Springer Publ. Berlin. 362 p.
159. L.I. Kurteeva, S.V. Morozov, A.G. Anshits
     Sources of carcinogenic PAH emission in aluminum production using Soderberg cell.
     // In: Advances in the Geological Storage of Carbon Dioxide, 2006, P. 57-65. // Eds. S. Lombardi, L.K. Altunina, S.E. Beaubien. NATO Science Series: Springer Publ. Berlin. 362 p.

2005

160. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
161. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
162. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
163. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
164. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
165. В.Н. Пармон, Т.Д. Федотова, В.А. Резников, А.П. Чупахин, С.В. Коренев, В.А. Емельянов, А.Я. Тихонов, Н.Г. Наумов
     Химия в НГУ. Пособие для абитуриентов
     Новосибирск, НГУ, 2005, 2-е изд., доп. и перераб., 296 с., 800 экз.
166. Волчо К.П., Рогоза Л.Н., Салахутдинов Н.Ф., Толстиков А.Г., Толстиков Г.А.
     «Препаративная химия терпеноидов. Часть 1. Бициклические монотерпеноиды»
     Издательство СО РАН (Издание осуществлено при финансовой поддержке РФФИ (проект № 05-03-46009) Объем 20 уч.-изд. л., 280 стр. Тираж 280 экз.
167. Дембицкий В.М., Толстиков Г.А.
     «Органические метаболиты лишайников».
     ISBN 5-7692-0772-8. Новосибирск: Издательство СО РАН, филиал «Гео», 2005. - 135 с. (Издание осуществлено при финансовой поддержке Российского фонда фундаментальных исследований (проект № 04-03-46008)), Тематический план выпуска изданий СО РАН на 2005 г., № 39. Формат 70 х 108 '/16. Усл. печ. л. 11,9. Уч.-изд. л. 9,1. Тираж 300 экз. Рецензенты:академик Б.А. Трофимов, доктор химических наук Н.Ф. Салахутдинов.0772-8. ISBN 5-7692-0772-8

2004

168. Л.М. Волкова, А.В. Шпатов
     Идентификация органических соединений физическими методами (пособие для студентов 3 курса Новосибирского государственного архитектурно-строительного университета (НГАСУ))
     Новосибирск, изд-во НГАСУ, 20042, 12 стр., 100 экз.

Обзоры, статьи в научных журналах

2021

1. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
2. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
3. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
4. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
5. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
6. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2
7. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
   Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
   Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309
8. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
   Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
   Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309
9. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
   Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
   Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309
10. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309
11. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309
12. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81
13. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81
14. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81
15. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81
16. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
17. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
18. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
19. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
20. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
21. A.A. Sonina,Ch. S. Becker, A. D. Kuimov,I. K. Shundrina,V. Yu. Komarov,M.S. Kazantsev
    Alkyl-substituted bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophenes: weakening of intermolecular interactions and additive-assisted crystallization†
    CrystEngComm, 2021, Advance article doi:10.1039/D0CE01794A, IF=3.117
22. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
23. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
24. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
25. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
26. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
27. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
28. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492
29. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
30. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
31. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
32. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
33. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
34. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
35. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
36. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889
37. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889
38. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889
39. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889
40. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
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61. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
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62. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
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63. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
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65. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
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66. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
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67. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
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68. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
69. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
70. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
71. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
72. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
73. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572
74. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
75. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
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76. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
77. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
78. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
79. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
80. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
81. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
82. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
83. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
84. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267
85. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
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148. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, N.A. Orlova, I.A. Malakhov, V.N. Berezhnaya, E.D. Savina, Y.P. Tsentalovich
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149. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, N.A. Orlova, I.A. Malakhov, V.N. Berezhnaya, E.D. Savina, Y.P. Tsentalovich
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150. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
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152. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
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153. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
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154. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
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190. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
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191. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
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192. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
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193. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
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194. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
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195. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
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196. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
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197. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
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198. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
     Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
     Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=3.763
199. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
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200. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
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201. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
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232. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
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238. S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
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     Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
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2020

241. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
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686. И.К. Шундрина, И.В. Олейник, В.И. Пастухов, Л.А. Шундрин, В.С. Черноносова, П.П. Лактионов
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691. A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
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699. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
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702. A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
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744. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
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745. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
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762. V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
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     Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
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     Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
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     Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
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     Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
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     Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
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     Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
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     High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
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817. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
     High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
     Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
818. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
     High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
     Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
819. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
     High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
     Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
820. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
     High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
     Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
821. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
     Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
     ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
822. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
     Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
     ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
823. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
     Biophotonics approach for the study of leukocyte activation
     Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
824. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
     Biophotonics approach for the study of leukocyte activation
     Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
825. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
     Biophotonics approach for the study of leukocyte activation
     Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
826. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
     Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
     Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
827. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
     Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
     Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
828. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
     Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
     Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
829. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
     Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
     Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
830. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
     Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
     Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
831. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
     In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
     Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
832. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
     In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
     Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
833. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
     In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
     Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
834. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
     In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
     Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
835. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
     In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
     Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
836. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
     Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
     Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
837. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
     Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
     Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
838. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
     Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
     Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
839. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
     Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
     Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
840. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
     Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
     European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
841. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
     Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
     European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
842. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
     Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
     European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
843. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
     Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
     European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
844. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
     Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
     European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
845. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
846. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
847. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
848. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
849. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
850. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
851. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
852. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
853. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
854. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
     No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
     ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
855. D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
     Study of calcium signaling dynamics in single platelets using optical activation methods.
     Proceedings of SPIE, 2020, V. 11359, #113590U doi:10.1117/12.2559414
856. D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
     Study of calcium signaling dynamics in single platelets using optical activation methods.
     Proceedings of SPIE, 2020, V. 11359, #113590U doi:10.1117/12.2559414
857. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
858. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
859. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
860. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
861. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
862. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
863. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
     Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
     Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
864. V.A. Logvinenko, V.P. Fadeeva, B.A. Selivanov, V.D. Tikhova, A.A. Nefedov, A.Ya. Tikhonov
     Thermal decomposition of several N,N'-bis(2-hydroxyiminoalkyl)-α,α'-dinitrones
     Journal of Thermal Analysis and Calorimetry, 2020, V. 140, N 2, Pp 685-693 doi:10.1007/s10973-019-08868-4, IF=2.731
865. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
866. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
867. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
868. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
869. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
870. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
871. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
872. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
873. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
     Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
     The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
874. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
     Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
     Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
875. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
     Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
     Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
876. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
     Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
     Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
877. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
     Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
     Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
878. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
     Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
     Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
879. D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
     Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
     Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
880. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
881. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
882. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
883. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
884. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
885. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
886. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
887. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
     (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
     Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
888. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
889. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
890. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
891. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
892. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
893. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
894. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
     Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
     The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
895. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
     Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
     Natural Product Research (Formerly Natural Product ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
896. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
     Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
     Natural Product Research (Formerly Natural Product ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
897. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
     Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
     Natural Product Research (Formerly Natural Product ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
898. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
     Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
     Natural Product Research (Formerly Natural Product ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
899. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
     Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
     Natural Product Research (Formerly Natural Product ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
900. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
     Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
     Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
901. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
     Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
     Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
902. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
     Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
     Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
903. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
     Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
     Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
904. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
     A search for synthetic routes to tetrabenzylglycoluril
     Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
905. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
     A search for synthetic routes to tetrabenzylglycoluril
     Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
906. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
     A search for synthetic routes to tetrabenzylglycoluril
     Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
907. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
     A search for synthetic routes to tetrabenzylglycoluril
     Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
908. А.В. Липеева, М.П. Долгих, Т.Г. Толстикова, Э.Э. Шульц
     Исследование растительных кумаринов. 18. конъюгаты кумаринов с лупановыми тритерпеноидами и 1,2,3-триазолами: синтез и противовоспалительная активность
     Биоорганическая химия. 2020. Т. 46. № 2. С. 115-123. DOI: 10.31857/S0132342320010194 (Study of Plant Coumarins. 18. Coumarin Conjugates with Lupane Triterpenoidsand 1,2,3-triazoles: Synthesis and Anti-inflammatory Activity/ Lipeeva A. V., Dolgikh М. Р., Tolstikova T. G., Shults E. E// Russian Journal of Bioorganic Chemistry, 2010, V. 46, N 2, Pp125-132 doi:10.1134/S1068162020010161), IF=0.682
909. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
     Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
     European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
910. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
     Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
     European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
911. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
     Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
     European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
912. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
     Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
     European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
913. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
     Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
     European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
914. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
     Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
     Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
915. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
     Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
     Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
916. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
     Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
     Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
917. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
     Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
     Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
918. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
     Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
     Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
919. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
920. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
921. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
922. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
923. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
924. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
     Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
     The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
925. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
     2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
     Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
926. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
927. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
928. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
929. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
930. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
931. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
932. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
933. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
934. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
935. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
936. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
     Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
     ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
937. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
     Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
     Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
938. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
     Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
     Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
939. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
     Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
     Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
940. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
     Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
     Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
941. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
     The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
     Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
942. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
     Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
     Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
943. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
     Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
     Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
944. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
     Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
     Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
945. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
     Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
     Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
946. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
     Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
     Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
947. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
     Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
     Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
948. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
     Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
     Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
949. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
     Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
     Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
950. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
     Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
     Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
951. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
     Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
     Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
952. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
     Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
     Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
953. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
     Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
     Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
954. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
     Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
     Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
955. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
     Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
     Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
956. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
     Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
     Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
957. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
958. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
959. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
960. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
961. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
962. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
     Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
     Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
963. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
     Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
     Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
964. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
     Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
     Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
965. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
966. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
967. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
968. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
969. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
970. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
971. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
972. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
973. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
974. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
     Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
     Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
975. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
     Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
     Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
976. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
     Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
     Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
977. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
     Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
     Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
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      Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
1021. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
      Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
      Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
1022. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
      Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
      Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
1023. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
      Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
      Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
1024. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
      Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
      Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
1025. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
      Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
      Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
1026. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
      Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
      Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
1027. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, С.А. Борисов, Т.Г. Толстикова, Д.Е. Семенов, М.А. Бакарев
      Простатотропное действие динатриевой соли глицирризиновой кислоты при моделировании доброкачественной гиперплазии предстательной железы
      Бюллетень экспериментальной биологии и медицины. 2020. Т. 169. № 1. С. 124-129. (Prostatotropic action of glycyrrhizic acid disodium salt in modeling benign prostatic hyperplasia/ Nizomov S.A., Sorokina I.V., Zhukova N.A., Borisov S.A., Tolstikova T.G., Semenov D.E., Bakarev M.A.// Bulletin of Experimental Biology and Medicine, 2020, V. 169, N 1, Pp 114-118 doi:10.1007/s10517-020-04836-3), IF=0.775
1028. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, С.А. Борисов, Т.Г. Толстикова, Д.Е. Семенов, М.А. Бакарев
      Простатотропное действие динатриевой соли глицирризиновой кислоты при моделировании доброкачественной гиперплазии предстательной железы
      Бюллетень экспериментальной биологии и медицины. 2020. Т. 169. № 1. С. 124-129. (Prostatotropic action of glycyrrhizic acid disodium salt in modeling benign prostatic hyperplasia/ Nizomov S.A., Sorokina I.V., Zhukova N.A., Borisov S.A., Tolstikova T.G., Semenov D.E., Bakarev M.A.// Bulletin of Experimental Biology and Medicine, 2020, V. 169, N 1, Pp 114-118 doi:10.1007/s10517-020-04836-3), IF=0.775
1029. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
      Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
      Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
1030. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
      Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
      Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
1031. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
      Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
      Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
1032. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
      Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
      Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
1033. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
      Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
      Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
1034. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
      Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
      Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
1035. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
      Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
      Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
1036. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1037. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1038. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1039. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1040. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1041. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
      Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
      Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
1042. L. Politanskaya, E. Tretyakov, Ch. Xi
      Synthesis of polyfluorinated o-hydroxyacetophenones - convenient precursors of 3-benzylidene-2-phenylchroman-4-ones
      Journal of Fluorine Chemistry, V. 229, January 2020, 109435 doi:10.1016/j.jfluchem.2019.109435, IF=2.332
1043. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
      Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
      Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209
1044. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
      Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
      Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209
1045. D. Spiryova, A. Vorob'ev, A.E. Moskalensky
      Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
      Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621
1046. D. Spiryova, A. Vorob'ev, A.E. Moskalensky
      Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
      Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621

2019

1047. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1048. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1049. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1050. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1051. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1052. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1053. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
      DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
      Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
1054. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
      Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
      Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
1055. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
      Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
      Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
1056. V.V. Bardin, N.Yu. Adonin
      The preparation of pentafluorophenyldihaloboranes from pentafluorophenylmercurials C6F5HgR and BX3: the dramatic dependence of the reaction direction on the ligand R
      Monatshefte für Chemie - Chemical Monthly, 2019, V.150, N 8, pp 1523-1531 doi:10.1007/s00706-019-02476-6, IF=1.501
1057. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1058. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1059. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1060. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1061. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1062. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
      One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
      Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
1063. S.V. Nikitin, J. Sanchez-Marquez, I.I. Oleynik, I. Oleynik, E.G. Bagryanskaya
      A screening DFT study of the para-substituent effect on local hyper-softness in bis(phenoxy-imine) titanium complexes to get insights about their catalytic activity in ethylene polymerization
      Molecular Catalysis, 2019, V. 469, Pp 57-67 doi:10.1016/j.mcat.2019.02.024, IF=2.938
1064. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
      Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
      The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
1065. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
      Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
      The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
1066. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
      Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
      The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
1067. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
      Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
      The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
1068. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
      Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
      The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
1069. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
      Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
      The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
1070. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
      Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
      The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
1071. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
      Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
      Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
1072. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
      Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
      Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
1073. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
      Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
      Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
1074. A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
      Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
      Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147
1075. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
      Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
      Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
1076. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
      Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
      Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
1077. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
      Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
      Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
1078. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
      Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
      Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
1079. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
      Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
      Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
1080. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
      Aromatic S_N^F-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
      Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
1081. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
      Aromatic S_N^F-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
      Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
1082. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1083. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1084. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1085. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1086. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1087. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
      Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
      Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
1088. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
      Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
      Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
1089. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
      Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
      Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
1090. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
      Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
      Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
1091. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
      Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
      Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
1092. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
      Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
      Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
1093. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
      Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
      RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
1094. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
      Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
      RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
1095. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
      Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
      RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
1096. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
      Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
      RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
1097. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
      Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
1098. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
      Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
1099. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
      Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
1100. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
      Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
1101. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
      The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
      Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
1102. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
      The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
      Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
1103. Н.А. Панкрушина, О.И. Ломовский, Т.П. Шахтшнейдер
      Физическая активация процессов экстракции и органического синтеза
      Химия в интересах устойчивого развития. 2019. Т. 27. № 6. С. 704-715. (Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194)
1104. Н.А. Панкрушина, О.И. Ломовский, Т.П. Шахтшнейдер
      Физическая активация процессов экстракции и органического синтеза
      Химия в интересах устойчивого развития. 2019. Т. 27. № 6. С. 704-715. (Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194)
1105. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
      Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
      Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
1106. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
      Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
      Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
1107. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
      Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
      Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
1108. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
      Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
      Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
1109. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
      Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
      Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
1110. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
      Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
      Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
1111. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
      Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
      Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
1112. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
      Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
      Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
1113. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
      Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
      Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
1114. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
      Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
      Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
1115. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
      Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
      Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
1116. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
      Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
      Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
1117. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
      Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
      Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
1118. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
      Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
      Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
1119. V.I. Borovkov, L.N. Shchegoleva
      Magnetic Resonance Characteristics of Negative Polarons in Neat Poly(3-hexyl-thiophene)
      Journal of Physical Chemistry C, 2019, 123, 46, 28058-28065 doi:10.1021/acs.jpcc.9b08331, IF=4.309
1120. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
      C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
      Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
1121. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
      C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
      Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
1122. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
      C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
      Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
1123. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
      C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
      Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
1124. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
      Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
      Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
1125. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
      Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
      Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
1126. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
      Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
      Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
1127. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
      Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
      Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
1128. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
      Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
      Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
1129. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
      Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
      Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
1130. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
      Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
      Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
1131. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
      Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
      Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
1132. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
      Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
      Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
1133. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1134. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1135. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1136. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1137. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1138. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1139. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1140. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1141. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1142. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
      Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
      UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
1143. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
      Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
      Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
1144. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
      Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
      Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
1145. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
      Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
      Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
1146. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1147. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1148. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1149. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1150. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1151. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1152. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1153. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1154. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
      Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
      Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
1155. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1156. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1157. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1158. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1159. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1160. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1161. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
      6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
      Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
1162. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1163. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1164. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1165. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1166. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1167. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1168. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
      Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
      Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
1169. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1170. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1171. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1172. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1173. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1174. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1175. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1176. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
      Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
      Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
1177. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
      Synthesis of benzo[c][1,7]naphthyridine derivatives
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
1178. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
      Synthesis of benzo[c][1,7]naphthyridine derivatives
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
1179. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
      Synthesis of benzo[c][1,7]naphthyridine derivatives
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
1180. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
      Synthesis of benzo[c][1,7]naphthyridine derivatives
      Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
1181. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
      Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
      Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
1182. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
      Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
      Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
1183. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1184. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1185. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1186. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1187. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1188. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1189. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
      Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
      Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
1190. М.В. Хвостов, Т.Г. Толстикова, С.А. Борисов, А.В. Душкин
      Применение природных полисахаридов в фармацевтике
      Биоорганическая химия, 2019, том 45, № 6, с. 563-575 (doi:10.1134/S0132342319060241) (Application of Natural Polysaccharides in Pharmaceutics/ M.V. Khvostov, T.G. Tolstikova, S.A. Borisov, A.V. Dushkin// Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 438-450 doi:10.1134/S1068162019060219), IF=0.794
1191. Т.П. Кукина, И.В. Хан
      Липофильные компоненты мытников PEDICULARIS STRIATA PALLAS и PEDICULARIS FLAVA PALLAS
      Химия растительного сырья. 2019. № 4. С. 113-118. (Lipophilic constituents of pedicularis striata pallas и pedicularis flava pallas/ Kukina, T.P., Khan, I.V.// Khimiya Rastitel'nogo Syr'ya, Issue 4, 1 January 2020, Pages 113-118 doi:10.14258/jcprm.2019044952)
1192. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
      Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
      Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
1193. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
      Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
      Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
1194. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
      Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
      Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
1195. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
      Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
      Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
1196. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
      Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
      Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
1197. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
      Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
      Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
1198. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
      Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
      Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
1199. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
      Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
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1200. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
      Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
      Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
1201. L. Politanskaya, N. Troshkova, E. Tretyakov, Ch. Xi
      Synthesis of polyfluorinated bezofurans
      Journal of Fluorine Chemistry, Volume 227, November 2019, 109371 doi:10.1016/j.jfluchem.2019.109371, IF=2.055
1202. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
      Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
      Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
1203. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
      Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
      Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
1204. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
      Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
      Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
1205. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1206. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1207. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1208. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1209. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1210. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1211. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1212. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1213. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1214. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1215. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1216. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1217. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
      Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
1218. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
      Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
      ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
1219. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
      Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
      ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
1220. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
      A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
      ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
1221. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
      A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
      ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
1222. S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
      Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
      Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136
1223. S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
      Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
      Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136
1224. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
      Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
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1225. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
      Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
      Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
1226. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
      Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
      Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
1227. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
      Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
      Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
1228. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
      Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
      Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
1229. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
      Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
      Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
1230. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
      Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
      Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
1231. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
      Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
      Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
1232. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
      Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
      Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
1233. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
      Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
      Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
1234. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
      Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
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1235. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
      Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
      New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
1236. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
      Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
      New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
1237. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
      Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
      New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
1238. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
      Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
      New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
1239. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
      Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
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1240. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
      Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
      Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
1241. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
      Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
      Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
1242. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
      Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
      Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
1243. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
      Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
      Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
1244. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
      Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
      Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
1245. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
      Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
      Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
1246. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
      Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
      Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
1247. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
      Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
      Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
1248. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
      Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
      Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
1249. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
      Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
      Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
1250. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
      Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
      Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
1251. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
      Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
      Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
1252. В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
      Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
      Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751
1253. В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
      Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
      Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751
1254. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
      Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
      Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
1255. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
      Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
      Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
1256. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
      Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
      Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
1257. E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
      Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
      Mendeleev Commun., 2019, V. 29, N 5, Pp 584-586 doi:10.1016/j.mencom.2019.09.036, IF=2.01
1258. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1259. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1260. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1261. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1262. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1263. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
      Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
      Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
1264. A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
      Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
      SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11
1265. A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
      Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
      SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11
1266. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
      Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
      Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
1267. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
      Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
      Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
1268. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
      Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
      Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
1269. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
      Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
      Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
1270. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
      Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
      CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
1271. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
      Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
      CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
1272. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
      Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
      MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
1273. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
      Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
      MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
1274. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
      Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
      MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
1275. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
      Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
      MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
1276. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1277. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1278. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1279. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1280. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1281. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
1282. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
      Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
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      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1287. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1288. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1289. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1290. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1291. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
      Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
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1292. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
      Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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      Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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1294. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
      Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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1295. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
      Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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1296. E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
      Chiral C₂-Symmetric Diimines with 4,5-Diazafluorene Units
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1297. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
      Oxidative addition of verdazyl halogenides to Pd(PPh3)4
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      Oxidative addition of verdazyl halogenides to Pd(PPh3)4
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1302. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
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1303. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
      The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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      The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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1305. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
      The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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1306. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
      The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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1307. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
      The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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1308. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1309. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1310. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
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1311. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1312. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1313. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1314. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
      Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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1315. E. Babaylova, A. Malygin, A. Gopanenko, D. Graifer, G. Karpova
      Tetrapeptide 60-63 of human ribosomal protein uS3 is crucial for translation initiation
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      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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1320. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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1321. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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1322. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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1323. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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      Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
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      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
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      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
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      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
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      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
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1333. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
      Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
      Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
1334. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1335. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1336. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1337. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1338. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1339. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1340. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
      Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
1341. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
      Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
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1342. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
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1343. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
      Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
1344. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
      Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
1345. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
      Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
1346. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
      Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
1347. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
      A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
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1348. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
      A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
      Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
1349. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
      A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
      Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
1350. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
      A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
      Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
1351. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
      A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
      Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
1352. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1353. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1354. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1355. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1356. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1357. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
      2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
      Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
1358. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
      Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
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1359. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
      Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
      Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567
1360. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
      Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
      Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567
1361. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, И.В. Ельцов
      Алифатические и тритерпеновые продукты омыления эфирных экстрактов POPULUS NIGRA L
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1362. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1363. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1364. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1365. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1366. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1367. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1368. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
      The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
1369. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
      The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
1370. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1371. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1372. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
      Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
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1373. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
      Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
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1374. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
      Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056
1375. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
      Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056
1376. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
      Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
1377. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
      Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
1378. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
      Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
1379. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
      Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
      IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
1380. Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
      Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
      Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595
1381. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
      Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
      Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
1382. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
      Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
      Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
1383. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
      Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
      Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
1384. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
      How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
      RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
1385. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
      How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
      RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
1386. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
      How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
      RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
1387. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
      How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
      RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
1388. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1389. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1390. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1391. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1392. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1393. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
      Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
      Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
1394. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
      Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
      Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
1395. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
      Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
      Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
1396. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
      Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
      Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
1397. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
      Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
      Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
1398. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
      The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
      Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
1399. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
      The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
      Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
1400. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
      The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
      Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
1401. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
      The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
      Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
1402. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
      The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
      Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
1403. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
      Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
      Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
1404. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
      Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
      Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
1405. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
      Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
      Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
1406. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
      Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
      Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
1407. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
      Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
      Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
1408. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1409. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1410. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1411. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1412. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1413. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
      Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
1414. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
      Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
      Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
1415. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
      Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
      Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
1416. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
      Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
      Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
1417. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
      Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
      Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
1418. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1419. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1420. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1421. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1422. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1423. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
      Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
      Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
1424. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1425. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1426. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1427. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1428. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1429. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1430. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
      Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
      Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
1431. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1432. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1433. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1434. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1435. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1436. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
      Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
      Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
1437. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
      EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
      Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
1438. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
      EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
      Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
1439. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
      EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
      Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
1440. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
      EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
      Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
1441. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
      EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
      Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
1442. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1443. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1444. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1445. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1446. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1447. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1448. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
      Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
      Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
1449. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
      Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
      Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
1450. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
      Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
      Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
1451. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
      Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
      Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
1452. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
      Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
      Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
1453. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1454. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1455. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1456. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1457. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1458. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1459. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1460. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
      The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
      Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
1461. A. Ochkasova, M. Meschaninova, A. Venyaminova, A. Ivanov, D. Graifer, G. Karpova
      The human ribosome as a possible mRNA quality controller that recognizes the abasic site by protein uS3
      FEBS OPEN BIO, V. 9, Pp 163-163, Suppl. 1 Аннотация к встрече: P-11-010, WOS:000486972402108, IF=1.958
1462. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
      Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
      JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
1463. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
      Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
      JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
1464. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
      Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
      JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
1465. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
      Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
      JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
1466. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1467. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1468. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1469. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1470. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1471. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1472. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
      Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
      Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
1473. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1474. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1475. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1476. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1477. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1478. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1479. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1480. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1481. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
      Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
      Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
1482. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1483. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1484. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1485. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1486. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1487. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1488. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1489. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1490. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1491. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
      Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
      J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
1492. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
      Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
      Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
1493. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
      Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
      Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
1494. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
      Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
      Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
1495. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
      Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
      Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
1496. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
      Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
      Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
1497. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
      Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
      Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
1498. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
      Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
      Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
1499. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
      Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
      Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
1500. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
      Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
      Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
1501. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
      Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
      Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
1502. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
      Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
      Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
1503. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
      Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
      Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
1504. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
      Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
      Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
1505. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
      Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
      Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
1506. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
      Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
      Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
1507. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
      Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
      Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
1508. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
      Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
      Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
1509. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
      Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
      Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
1510. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
      Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
      Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
1511. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
      Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
      Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
1512. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
      Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
      Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
1513. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
      Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
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1514. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1515. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1516. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1517. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1518. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1519. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1520. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1521. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1522. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
      Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
      Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
1523. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1524. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1525. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1526. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1527. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1528. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
      Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
      Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
1529. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
      Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
      Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
1530. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
      Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
      Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
1531. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
      Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
      Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
1532. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1533. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1534. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1535. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1536. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1537. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
      Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
      Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
1538. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1539. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1540. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1541. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1542. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1543. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1544. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1545. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1546. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1547. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
      Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
      Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
1548. V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
      Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
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1549. V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
      Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
      Journal of Soils and Sediments, 2019, V. 19, N 6, pp 2697-2707 doi:10.1007/s11368-018-2097-x, IF=2.669
1550. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
      Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
      Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
1551. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
      Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
      Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
1552. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
      Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
      Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
1553. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
      Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
      Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
1554. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1555. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1556. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1557. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1558. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1559. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1560. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1561. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
      Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
      Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
1562. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Д.Е. Семенов, А.Е. Просенко
      Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
      Бюллетень экспериментальной биологии и медицины. 2019. Т. 167. № 6. С. 772-776. (Morphological analysis of prostatotropic activity of (3,5-dimethyl-4-hydroxy) benzyltiodyododecan in the model of benign prostatic hyperplasia in rats/ S.A. Nizomov, I.V. Sorokina, N.A. Zhukova, T.G. Tolstikova, D.E. Semenov, A.E. Prosenko// Bulletin of Experimental Biology and Medicine, 2019, V. 167, N 6, pp 809-812 doi:10.1007/s10517-019-04628-4), IF=0.567
1563. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Д.Е. Семенов, А.Е. Просенко
      Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
      Бюллетень экспериментальной биологии и медицины. 2019. Т. 167. № 6. С. 772-776. (Morphological analysis of prostatotropic activity of (3,5-dimethyl-4-hydroxy) benzyltiodyododecan in the model of benign prostatic hyperplasia in rats/ S.A. Nizomov, I.V. Sorokina, N.A. Zhukova, T.G. Tolstikova, D.E. Semenov, A.E. Prosenko// Bulletin of Experimental Biology and Medicine, 2019, V. 167, N 6, pp 809-812 doi:10.1007/s10517-019-04628-4), IF=0.567
1564. A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
      Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
      Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541
1565. A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
      Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
      Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541
1566. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
      Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
      J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
1567. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
      Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
      J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
1568. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1569. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1570. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1571. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1572. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1573. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1574. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
      Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
      International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
1575. T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
      Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
      Journal of Antibiotics, 2019, V. 72, pp 590-599 doi:10.1038/s41429-019-0191-y, IF=2.446
1576. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
      Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
      Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
1577. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
      Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
      Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
1578. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
      Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
      Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
1579. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1580. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1581. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1582. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1583. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1584. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1585. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
      Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
      Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
1586. D. Stass, E. Tretyakov
      Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
      Magnetochemistry, 2019, 5(2), 32 (This article belongs to the Special Issue Controlling Molecular Nanomagnets) doi:10.3390/magnetochemistry5020032
1587. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1588. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1589. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1590. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1591. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1592. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1593. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1594. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1595. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1596. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
      Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
      Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
1597. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
      Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
      Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
1598. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
      Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
      Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
1599. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
      Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
      Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
1600. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
      Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
      Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
1601. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
      Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
      Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
1602. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1603. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1604. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1605. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1606. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1607. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1608. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1609. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1610. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1611. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1612. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
      Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
      Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
1613. N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
      p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
      Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08
1614. N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
      p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
      Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08
1615. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
      International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
1616. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
      International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
1617. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
      International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
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      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
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1619. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
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1620. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
      Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
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1621. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
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      Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
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      Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
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      Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
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      Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
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      Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
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      Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
      Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014
1639. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
      Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
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      Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
      Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014
1641. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
      Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
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      Влияние алифатических диолов и дикарбоновых кислот на свойства сополиэфиров этиленсукцината
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      О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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1644. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
      О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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1645. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
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1646. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
      О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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