Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 76, Issue 4, Pages 1174-1176Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo1023377
Keywords
-
Categories
Funding
- National Institutes of Health [GM-46059, 1F32GM093532]
- EMD Serono
- Martin Family Society of Fellows for Sustainability
- National Science Foundation (NSF) [CHE-9808061, DBI-9729592]
Ask authors/readers for more resources
A method for the room temperature copper-mediated trifluoromethylation of aryl and heteroaryl boronic acids has been developed. This protocol is amenable to normal benchtop setup and reactions typically require only 1-4 h. Proceeding under mild conditions, the method tolerates a range of functional groups, allowing access to a variety of trifluoromethylarenes.
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