Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 50, Pages 18706-18709Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja411647x
Keywords
-
Categories
Funding
- CREST from JST
- NEXT program
- Program for Leading Graduate Schools Integrative Graduate Education and Research Program in Green Natural Sciences in Nagoya University
- Daiko Foundation
Ask authors/readers for more resources
A highly diastereo- and enantioselective ring-opening alkylation of racemic 2,2-disubstituted aziridines with 3-substituted oxindoles is achieved under the catalysis of a chiral 1,2,3-triazolium salt. This reaction represents a hitherto unknown, catalytic stereoselective carbon carbon bond formation through direct substitution at the tetrasubstituted chiral carbon.
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