Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 3, Issue 10, Pages 1345-1349Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6qo00139d
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Funding
- Grants-in-Aid for Scientific Research [15K13689, 16H06038, 26288045] Funding Source: KAKEN
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Photoredox catalysis has emerged as a strong synthetic tool for radical reactions. In particular, a variety of regioselective difunctionalizations of carbon-carbon multiple bonds through SET photoredox processes (oxidative quenching cycle) have been accomplished by an appropriate choice of an electrophilic radical precursor and a nucleophile. The basic concept, representative results and future prospect are the topics of this article.
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