Current trends towards the synthesis of bioactive heterocycles and natural products using 1, 3-dipolar cycloadditions (1, 3-DC) with azomethine ylides

HA Döndas, M de Gracia Retamosa, JM Sansano - Synthesis, 2017 - thieme-connect.com
This review summarizes the trends in the formation of complex or not so complex
heterocyclic structures through 1, 3-dipolar cycloadditions of azomethine ylides. Diastereo …

Azomethine Ylides—Versatile Synthons for Pyrrolidinyl-Heterocyclic Compounds

SS Panda, MN Aziz, J Stawinski, AS Girgis - Molecules, 2023 - mdpi.com
Azomethine ylides are nitrogen-based three-atom components commonly used in [3+ 2]-
cycloaddition reactions with various unsaturated 2π-electron components. These reactions …

Modern Trends of Organic Chemistry in Russian Universities

AI Konovalov, IS Antipin, VA Burilov… - Russian Journal of …, 2018 - Springer
This review is devoted to the scientific achievements of the departments of organic chemistry
in higher schools of Russia within the past decade.

Synthesis and biological properties of nitrobenzoxadiazole derivatives as potential nitrogen(ii) oxide donors: SOX induction, toxicity, genotoxicity, and DNA protective activity in …

VA Chistyakov, YP Semenyuk, PG Morozov… - Russian Chemical …, 2015 - Springer
Dihetaryls containing superelectrophilic and π-excessive heterocycles were synthesized by
the nucleophilic aromatic substitution and cycloaddition. The structures of the compounds …

Sequential SNAr and Diels–Alder reactivity of superelectrophilic 10π heteroaromatic substrates

YP Semenyuk, PG Morozov, ON Burov, ME Kletskii… - Tetrahedron, 2016 - Elsevier
Using the DFT concept of global electrophilicity (ω), it is shown that 4, 6-dinitro-7-chloro-
benzo-furoxan and-benzofurazan are two 10π-heteroaromatics that rank to the top of the ω …

Синтез и биологические свойства производных нитробензоксадиазолов-потенциальных доноров оксида азота (II): SOX-индукция, токсичность …

ВА Чистяков, ЮП Семенюк, ПГ Морозов… - … Академии наук. Серия …, 2015 - elibrary.ru
Методами нуклеофильного ароматического замещения и циклоприсоединения
синтезированы дигетарилы, включающие суперэлектрофильные и π-избыточные …

Mechanisms for the formation of five-membered rings in ethene addition reactions with azomethine ylide and allyl anion

ME Kletskii, ON Burov, NS Fedik… - Chemistry of Heterocyclic …, 2016 - Springer
The mechanisms of pyrrolidine and cyclopentyl anion formation in the ethene addition
reactions to allyl anion and azomethine ylide, as well as to their derivatives with π-electron …

Механизмы образования пятичленных циклов в реакциях присоединения этилена к азометин-илиду и аллил-аниону

МE Клецкий, ОН Буров, НC Федик… - Chemistry of Heterocyclic …, 2016 - hgs.osi.lv
Для широкого круга систем при помощи расчетов ab initio в базисе MP2/6-311++ G (d, p)
проведено сравнительное изучение механизмов образования пирролидина и …