ChemistrySelect, 2024, 9(18)

[3+2] Cycloaddition of N-benzylazomethine Methylide with Various Arylidene-Azolones

Spirocyclic skeletons are highly attractive for design of biologically active compounds. [3+2] Cycloaddition of N-benzylazomethine methylide with various arylidene-azolones achieve to synthesize promising series of substituted spirocyclic structures. Systematic study of the scope and stereochemical outcome of [3+2]-cycloaddition was performed.

Tiushina IV, Sokolov AI, Smirnov AY, Dubinnyi MA, Ivanov DS, Korlyukov AA, Mikhaylov AA, Baranov MS

Laboratory of biomolecular NMR-spectroscopy, Laboratory of chemistry of heterocyclic compounds, Group of chemistry of natural products

: 10.1002/slct.202400930
Scopus: 2-s2.0-85192059249
IBCH: 11321
Ссылка на статью в журнале: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.202400930
Кол-во цитирований на 08.2026: 3
Данные статьи проверены модераторами 2024-09-21

Список научных проектов, где отмечена публикация

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