4.7 Article

Enantioselective synthesis of highly functionalised amides by copper-catalysed vinylogous Mukaiyama aldol reaction

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 30, Pages 5497-5499

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc00996b

Keywords

-

Funding

  1. Fonds der Chemischen Industrie

Ask authors/readers for more resources

Amides with quaternary stereogenic centers have been synthesised by catalytic asymmetric vinylogous Mukaiyama aldol reactions. The chiral copper-sulfoximine catalyst gives rise to products with moderate to good yields and up to 92% ee.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available