Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 7, Pages 2452-2455Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja512746q
Keywords
-
Categories
Funding
- NIH [GM095666]
- Sloan Foundation
Ask authors/readers for more resources
We report the highly enantioselective addition of photogenerated alpha-amino radicals to Michael acceptors. This method features a dual-catalyst protocol that combines transition metal photoredox catalysis with chiral Lewis acid catalysis. The combination of these two powerful modes of catalysis provides an effective, general strategy to generate and control the reactivity of photogenerated reactive intermediates.
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