Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 81, Issue 3, Pages 860-867Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b02433
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Funding
- Natural Science Basic Research Plan in Shaanxi Province of China [2014JQ2071]
- Fundamental Research Funds of the Central Universities [2015qngz17]
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An efficient palladium-catalyzed alkylarylation of acrylamides with unactivated alkyl halides has been developed. This method is highlighted by its broad substrate scope and excellent functional group tolerance. In addition to alkyl halides, fluoroalkyl halides and benzyl bromides also participated well in this transformation. A detailed mechanistic investigation suggests that a radical pathway is probably involved in the cyclization process.
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