Journal
ORGANIC LETTERS
Volume 15, Issue 15, Pages 3990-3993Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol401779h
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- MEXT
- JSPS
- JST, Japan
- Grants-in-Aid for Scientific Research [25105733, 25288048] Funding Source: KAKEN
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The ruthenium-catalyzed alkenylation reactions of 2-aminobiphenyls and cumylamine proceed smoothly to produce the corresponding regioselectively alkenylated products. These reactions involve a C-H bond cleavage directed by their free amino groups.
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