Journal
CHEMICAL COMMUNICATIONS
Volume 59, Issue 51, Pages 7943-7946Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc02317f
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A dinuclear gold-catalyzed radical difunctionalization of alkyl bromides with 1,7-enynes has been developed via dehalogenation and 1,5-HAT processes. This protocol efficiently constructs cyclopenta[c]quinolines bearing two quaternary carbon centers with good yields (28 examples, up to 84% yield). The reaction exhibits excellent functional group compatibility and scalability, demonstrating its synthetic robustness.
Dinuclear-gold-catalyzed radical difunctionalization of alkyl bromides with 1,7-enynes has been established via dehalogenation and 1,5-HAT processes. This protocol was used to construct, in a facile and efficient manner, a wide range of cyclopenta[c]quinolines bearing two quaternary carbon centers with good yields (28 examples, up to 84% yield). The good functional group compatibility and gram-scale preparation ability of the reaction proved its synthetic robustness.
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