Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides

Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.

Saved in:
Bibliographic Details
Published in:Chemical communications (Cambridge, England) England), 2009-01 (7), p.833-835
Main Authors: Zhang, Xue-Jing, Liu, Sheng-Ping, Li, Xue-Ming, Yan, Ming, Chan, Albert S C
Format: Article
Language:English
Subjects:
Aldehydes - chemistry
Alkenes - chemistry
Amines - chemistry
Catalysis
Cross-Linking Reagents - chemical synthesis
Cross-Linking Reagents - chemistry
Stereoisomerism
Substrate Specificity
Sulfonamides - chemistry
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Chiral bifunctional sulfamides were found to be highly efficient organocatalysts for the conjugate addition of aldehydes to nitroolefins in the presence of base additives.
ISSN:1359-7345
1364-548X
DOI:10.1039/b818582d