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Vol. 58 No. 2/3 (2022)
Vol. 58 No. 2/3 (2022)
2022 № 2/3 (656/657) p. 73–158
Published:
2022-03-10
Review Articles
SYNTHESIS OF TETRAZOLE DERIVATIVES THROUGH CONVERSION OF AMIDE AND THIOAMIDE FUNCTIONALITIES
Naimish Verma, Smritilkha Bera, Dhananjoy Mondal
73-83
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ELECTROPHILIC FLUORINATION OF HETEROCYCLIC COMPOUNDS WITH NF REAGENTS IN UNCONVENTIONAL MEDIA
Геннадий И. Бородкин, Вячеслав Г. Шубин
84-96
PDF (Русский)
Heterocycles in Focus
CHEMOSENSORS BASED ON 5-ETHYLIDENE-SUBSTITUTED BARBITURIC ACID DERIVATIVES
Nelli Batenko, Anastasija Gaile
97-99
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Original Papers
SYNTHESIS OF POLYMETHOXYFLAVONOIDS FROM HESPERIDIN AND NARINGIN AND THEIR ANTIPROLIFERATIVE ACTIVITY
Liang Su, Zhizhong Jin, Kexiong Liu, Qiuan Wang
100-105
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SYNTHESIS OF MONOSUBSTITUTED TRIFLUOTOMETHYLATED DERIVATIVES OF 2
H
-THIETE, DIHYDROTHIOPHENES AND 2
H
-THIOPYRANES
Сергей A. Сирый, Вадим M. Тимошенко, Тимофей B. Руденко, Юрий H. Маркитанов, Эдуард Б. Русанов, Юрий Г. Шермолович
106-115
PDF (Русский)
EXPANDING THE CHEMICAL SPACE OF 3(5)-FUNCTIONALIZED 1,2,4-TRIAZOLES
Dmytro M. Khomenko, Roman O. Doroshchuk, Yulia M. Ohorodnik, Hanna V. Ivanova, Borys V. Zakharchenko, Ilona V. Raspertova, Oleksandr V. Vaschenko, Alexey V. Dobrydnev, Oleksandr O. Grygorenko, Rostyslav D. Lampeka
116-128
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N
-3,3,3-TRIFLUOROPROPENYL DERIVATIVES OF AZOLES
Кирилл И. Петко, Андрей А. Филатов, Юрий Л. Ягупольский
129-134
PDF (Русский)
SYNTHESIS OF CHIRAL PINOPYRIDINES USING CATALYSIS BY METAL COMPLEXES
Юлия П. Устименко, Александр М. Агафонцев, Алексей В. Ткачев
135-143
PDF (Русский)
NEW 13-VINYL DERIVATIVES OF BERBERINE: SYNTHESIS AND CHARACTERIZATION
Олег Д. Демёхин, Олег Н. Буров, Михаил Е. Клецкий, Антон В. Лисовин, Сергей В. Курбатов, Березняк Е. Александровна, Алёна В. Тришина
144-152
PDF (Русский)
Short Communications
OPENING OF THE 1,3,5-TRIAZINE RING IN 3-METHYL-5-(TRINITROMETHYL)TETRAZOLO[1,5-
a
][1,3,5]TRIAZIN-7-ONE BY THE ACTION OF ALCOHOLS
Владимир В. Бахарев, Александр А. Гидаспов, Владимир А. Заломленков, Виктор Е. Парфенов, Ольга В. Головина, Павел А. Слепухин
153-158
PDF (Русский)
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