4.7 Article

Oxidative Tandem Cyclization of Glycine Esters with Propargyl Alcohols

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JOURNAL OF ORGANIC CHEMISTRY
卷 88, 期 14, 页码 10232-10241

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.3c00627

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A facile and efficient aerobic oxidative (4 + 2)-cyclization/aromatization/lactonizationtandem reaction of N-aryl glycine esters with propargylalcohols to access quinoline-fused lactones is reported. The reactioncan be extended to homopropargylic alcohols too. The transformationis straightforward to perform under mild conditions and scalable,and both reaction components are readily available.
A facile and efficient aerobic oxidative (4 + 2)-cyclization/aromatization/lactonizationtandem reaction of N-aryl glycine esters with propargylalcohols to access quinoline-fused lactones is reported. The reactioncan be extended to homopropargylic alcohols too. The transformationis straightforward to perform under mild conditions and scalable,and both reaction components are readily available.

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