|
This article is cited in 12 scientific papers (total in 12 papers)
Vicarious nucleophilic substitution of hydrogen in electrophilic aldimines: synthesis of enamines substituted with electron-withdrawing groups
M. Makosza, Sh. Nizamov, A. Kwast Institute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland
Abstract:
Strongly electrophilic benzaldimines react with α -chlorocarbanions giving two types of substituted enamines, via vicarious nucleophilic substitution of hydrogen or a cyclisation-ring opening process.
Citation:
M. Makosza, Sh. Nizamov, A. Kwast, “Vicarious nucleophilic substitution of hydrogen in electrophilic aldimines: synthesis of enamines substituted with electron-withdrawing groups”, Mendeleev Commun., 6:2 (1996), 43–44
Linking options:
https://www.mathnet.ru/eng/mendc4904 https://www.mathnet.ru/eng/mendc/v6/i2/p43
|
|