Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 41, Pages 14626-+Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja906291n
Keywords
-
Categories
Funding
- NSFC [20621091, 2067204, 0732002]
- Chang Jiang Scholars Program
Ask authors/readers for more resources
The catalytic enantioselective synthesis of all-carbon quaternary stereogenic centers in spirocyclic diketones has been achieved for the first time by an unprecedented asymmetric vinylogous alpha-ketol rearrangement in which an enantiocontrotled semipinacol-type 1,2-carbon migration was realized using multifunctional cinchona-modified primary amine catalysis.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available