4.8 Article

Rh(III)-Catalyzed Enaminone-Directed C-H Coupling with α-Diazo-α-phosphonoacetate for Reactivity Discovery: Fluoride-Mediated Dephosphonation for C-C Coupling Reactions

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ORGANIC LETTERS
卷 20, 期 13, 页码 3819-3823

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b01406

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资金

  1. National Natural Science Foundation of China [21425415, 21774056]
  2. National Basic Research Program of China [2015CB856303]

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Rh(III)-catalyzed enaminone-directed C-H coupling with alpha-diazo-alpha-phosphonoacetate has been used for the identification of fluoride-mediated dephosphonation C-C coupling reactivity for the synthesis of 4-hydroxy-1-naphthoates. Intermolecular C-C coupling of alpha-phosphonoacetate and benzaldehyde for (E)-selective alpha,beta-unsaturated ester synthesis has also been achieved.

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