Федеральное государственное бюджетное учреждение науки
Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук

научных сотрудников Института:
Д.О. Приму, к.х.н. А.Г. Макарова, д.х.н. И.Ю. Багрянскую, д.б.н. Д.С. Баева, к.х.н. Т.Ф. Елисееву, к.х.н. Л.В. Политанскую, д.х.н. А.Ю. Макарова, д.х.н. А.В. Зибарева

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We are excited to share that your research, published in ChemistrySelect is among the top 10% most downloaded papers!

Prima D.O., Makarov A.G., Bagryanskaya I.Yu., Kolesnikov A.E., Zargarova L.V., Baev D.S., Eliseeva T.F., Politanskaya L.V., Makarov A.Yu., Slizhov Yu.G., Zibarev A.V.,

Fluorine-containing n-6 and angular and linear n-6-n’ (n, n’ = 5, 6, 7) diaza-heterocyclic scaffolds assembled on benzene core in unified way,

ChemistrySelect, 2019, 4, 2383-2386.
DOI: 10.1002/slct.03970.

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Fluorine‐Containing n‐6 and Angular and Linear n‐6‐n’ (n, n’ = 5, 6, 7) Diaza‐Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way

Darya O. Prima, Dr. Arkady G. Makarov, Prof. Dr. Irina Yu. Bagryanskaya, Andrey E. Kolesnikov, Leila V. Zargarova,  Dr. Dmitry S. Baev, Dr. Tatiana F. Eliseeva, Dr. Larisa V. Politanskaya, Dr. Alexander Yu. Makarov, Dr. Yuri G. Slizhov, Prof. Dr. Andrey V. Zibarev

ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386
First published: 27 February 2019


slct201803970 toc 0001 m


The title compounds, including hybrids (n ≠ n’), were assembled on benzene core in a unified way based on only one starting material C6F5NH2 and a limited number of simple substitution and condensation reactions. The heterocyclic moieties were 1,3‐diazoles, 1,2,3‐triazoles, 1,2,5‐thia(selena)diazoles, 1.4‐diazines and 1,5‐diazepines, as well as 1,3,2‐dioxaboroles. Representatives of all new scaffolds were characterized by XRD. Compounds synthesized are of biomedical interest in the context of apoptotic anticancer activity, and the 1,2,5‐thiadiazole/1,3,2‐dioxaborole hybrid also in that of neutron or/and proton capture therapy of cancer. New 1,2,5‐chalcogenadiazoles are protected forms of otherwise hardly accessible fluorine‐containing di‐ and tetra‐amines for further syntheses.


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