z-logo
Premium
Chiral‐Auxiliary‐Controlled Diastereoconvergent Benzamidation Reactions of Diastereomixtures of Diarylmethanols with Benzamide Catalyzed by SnBr 4
Author(s) -
Kubo Rikiya,
Nakata Kenya
Publication year - 2019
Publication title -
asian journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.846
H-Index - 44
eISSN - 2193-5815
pISSN - 2193-5807
DOI - 10.1002/ajoc.201800635
Subject(s) - benzamide , chemistry , substituent , catalysis , lewis acids and bases , combinatorial chemistry , organic chemistry , stereochemistry
An efficient chiral‐auxiliary‐controlled diastereoconvergent benzamidation reaction of diastereomixtures of diarylmethanols catalyzed by SnBr 4 (Lewis acid) is described. A variety of substrates with various substituents on aromatic rings were applicable for the reaction, regardless of the type of substituent that they were bearing.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here