4.8 Article

Highly Enantioselective Organocatalyzed Vinylogous Michael-Type Reaction for the Construction of Trifluoromethylated All-Carbon Quaternary Stereocenters

Journal

ORGANIC LETTERS
Volume 16, Issue 5, Pages 1394-1397

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol500157b

Keywords

-

Funding

  1. NSFC [91213303, 21102141, 21272107, 21202072]
  2. National S&T Major Project of China
  3. Fundamental Research Funds for the Central Universities [860976, 861188]

Ask authors/readers for more resources

The first example of a highly enantioselective vinylogous Michael-type reaction of beta,beta-disubstituted nitroalkenes is disclosed. A series of biologically important chiral oxindoles, featuring a trifluoromethylated all-carbon quaternary chiral center, were obtained in good yields with excellent enantioselectivities (up to >99% 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

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available