4.7 Article

PPh3-Triggered Tandem Synthesis of 2,3-Disubstituted Benzofuran Derivatives from o-Quinone Methides with Acyl Chlorides

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JOURNAL OF ORGANIC CHEMISTRY
卷 87, 期 17, 页码 11852-11856

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.2c00910

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  1. National Natural Science Foundation of China [21702121]
  2. 111 Project [D20015]

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A PPh3-triggered tandem strategy has been developed for the efficient synthesis of valuable 2,3-disubstituted benzofuran derivatives from aryl or alkyl acyl chlorides and o-quinone methides. This method features mild reaction conditions, simple operation, and a broad substrate scope.
A PPh3-triggered tandem strategy for the efficient synthesis of valuable 2,3-disubstituted benzofuran derivatives in generally good to high yields from aryl or alkyl acyl chlorides and o-quinone methides has been developed. This method features mild reaction conditions, simple operation, and a broad substrate scope.

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