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A lesson for site-selective C-H functionalization on 2-pyridones: radical, organometallic, directing group and steric controls

期刊

CHEMICAL SCIENCE
卷 9, 期 1, 页码 22-32

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc04509c

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资金

  1. JSPS KAKENHI [JP 15H05485, JP 17H06092]
  2. Grants-in-Aid for Scientific Research [17H06092] Funding Source: KAKEN

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A 2-pyridone ring is a frequently occurring subunit in natural products, biologically active compounds, and pharmaceutical targets. Thus, the selective synthesis of substituted 2-pyridone derivatives through decoration and/or formation of pyridone rings has been one of the important longstanding subjects in organic synthetic chemistry. This minireview focuses on recent advances in site-selective C-H functionalization on 2-pyridone. The reported procedures are categorized according to the site selectivity that is achieved, and the substrate scope, limitations, mechanism, and controlling factors are briefly summarized.

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