Latest News
Web Date: March 29, 2012

New Class Of Superbases

Catalysis: Cyclopropenimines act as enantioselective catalysts
Department: Science & Technology
News Channels: JACS In C&EN, Organic SCENE
Keywords: organocatalysis, superbases, cyclopropenimines

Cyclopropenimines can serve as highly effective “superbases” for enantioselective organocatalysis, researchers have discovered (J. Am. Chem. Soc., DOI: 10.1021/ja3015764). The findings could lead to easier and faster syntheses of novel chiral compounds for drug discovery and other applications.

In recent years, researchers have developed several types of organic bases to catalyze enantioselective proton-transfer reactions and yield optically enriched products. Most work has focused on chiral amidines and guanidines, but these species have limited . . .

To view the rest of this content, please log in with your ACS ID.

Chemical & Engineering News
ISSN 0009-2347
Copyright © American Chemical Society