4.8 Article

Chiral Tetraaminophosphonium Carboxylate-Catalyzed Direct Mannich-Type Reaction

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 43, Pages 14088-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja806311e

Keywords

-

Funding

  1. Kurata Memorial Hitachi Science and Technology Foundation
  2. Nagoya University
  3. MEXT, Japan

Ask authors/readers for more resources

The cooperative asymmetric catalysis of chiral tetraaminophosphonium carboxylate (P,S)-1-OCOR has been established, and its synthetic utility has been successfully demonstrated by application to the highly enantioselective direct Mannich-type reaction of azlactones with N-sulfonyl imines. The present study stimulates the cultivation of the potential of the chiral quaternary onium salt catalysis by the structural modification of organic anion.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available