Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
51735 | Catalysis Communications | 2009 | 5 Pages |
Abstract
The chemoselective electrophilic substitution of electron rich arenes with N-(acyl)benzaldimines to benzhydrylamides proceeds smoothly under mild conditions (room temperature) in the presence of catalytic amounts of both homogeneous (binaphthol-phosphoric acid) and heterogeneous (Amberlyst-36) catalysts. The investigations revealed influences of the catalyst type on the reaction and the product spectrum.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Jens Deutsch, Marek Checinski, Angela Köckritz, Matthias Beller,