Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- V.V. Chernyshov, I.I. Popadyuk, O.I. Yarovaya, N.F. Salakhutdinov
Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
Topics in Current Chemistry, 2022, V. 380, Art. number: 42 doi:10.1007/s41061-022-00399-1, IF=8.904
- V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
- V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94
- 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
- V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 763-768 doi:10.1007/s10593-020-02728-y, IF=1.491
- 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