4.7 Article

Direct Arylation of Sydnones with Aryl Chlorides toward Highly Substituted Pyrazoles

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JOURNAL OF ORGANIC CHEMISTRY
卷 80, 期 4, 页码 2467-2472

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b00143

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  1. Cancer Research UK
  2. Yorkshire Cancer Research

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The direct arylation of the C4 position of both N-alkyl- and N-arylsydnones with aryl/heteroaryl chlorides has been realized. The reaction is quite general and allows access to a wide range of 4-substituted sydnones. Yields of more challenging substrates can be improved through the use of aryl bromides.

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