Journal
ORGANIC LETTERS
Volume 21, Issue 12, Pages 4853-4858Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01747
Keywords
-
Categories
Funding
- NSF [CHE-1664818]
- NIGMS [R01 GM 113878]
- National Natural Science Foundation of China [21602017]
- Natural Science Foundation of Jiangsu Province [BK20160405]
- University Science Research Project of Jiangsu Province [16KJB150001]
- China Scholarship Council [201708320115]
- Swedish Chemical Society
Ask authors/readers for more resources
A redox-neutral alkyl Petasis reaction has been developed that proceeds via photoredox catalysis. A diverse set of primary, secondary, and tertiary alkyltrifluoroborates participate effectively in this reaction through a single-electron transfer mechanism, in contrast to the traditional two-electron Petasis reaction, which accommodates only unsaturated boronic acids. This protocol is ideal to diversify benzyl-type and glyoxalate-derived aldehydes, anilines, and alkyltrifluoroborates toward the rapid assembly of libraries of higher molecular complexity important in pharmaceutical and agrochemical settings.
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