Journal
ORGANIC LETTERS
Volume 19, Issue 13, Pages 3430-3433Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01391
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Funding
- National Natural Science Foundation of China [21474048, 21372114, 21672099, 21472084]
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A hydroacylation reaction of alkenes has been achieved employing readily available carboxylic acids as the acyl source and hydrosilanes as a hydrogen source via photoredox catalysis. The combination of both single electron transfer and hydrogen atom transfer steps has dramatically expanded new applications of carboxylic acids in organic synthesis. The protocol also features extremely mild conditions, broad substrate scope, and good functional group tolerance, affording a novel and convenient approach to hydroacylation of alkenes.
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