Journal
ORGANIC LETTERS
Volume 16, Issue 9, Pages 2346-2349Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol500661t
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Funding
- Japan Society for the Promotion of Science (JSPS)
- Global COE Program (Chemistry Innovation through Cooperation of Science and Engineering)
- University of Tokyo
- Japan Science and Technology Agency (JST)
- Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
- Grants-in-Aid for Scientific Research [26810017] Funding Source: KAKEN
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A metal-free cross-dehydrogenative (CDC) reaction of tertiary amines was developed using a catalytic amount of sulfuryl chloride (SO2Cl2) under mild aerobic conditions. On the basis of the nature of SO2Cl2, it was assumed that the reagent acts as a radical initiator to induce the metal-free CDC reaction via a radical-initiated autoxidation mechanism.
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