[3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones
Author(s) -
Maxim E. Kukushkin,
Alexandra A. Kondratieva,
Н.А. Карпов,
Dmitry E. Shybanov,
В. А. Тафеенко,
Vitaly A. Roznyatovsky,
Yuri K. Grishin,
Anna A. Moiseeva,
N. V. Zyk,
Елена К. Белоглазкина
Publication year - 2022
Publication title -
royal society open science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 51
ISSN - 2054-5703
DOI - 10.1098/rsos.211967
Subject(s) - pyrrolidine , chemistry , cycloaddition , azomethine ylide , combinatorial chemistry , aryl , medicinal chemistry , organic chemistry , catalysis , 1,3 dipolar cycloaddition , alkyl
A synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substitutedα -amino acids has been developed.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom