Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 35, Pages 11270-11273Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b07678
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Funding
- NSF [CHE1265964]
- NIHGMS [R01-GM098601, R01-GM078201]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1265964] Funding Source: National Science Foundation
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Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible light photoredox conditions. Using these precursors, the first net redox-neutral coupling of tertiary and secondary alcohols with electron-deficient alkenes is achieved.
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