4.8 Article

Co(acac)2/O2-Mediated Oxidative Isocyanide Insertion with 2-Aryl Anilines: Efficient Synthesis of 6-Amino Phenanthridine Derivatives

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ORGANIC LETTERS
卷 16, 期 4, 页码 1260-1263

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AMER CHEMICAL SOC
DOI: 10.1021/ol500286x

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资金

  1. Natural Science Foundation of China [21172162, 21372174]
  2. Ph.D. Programs Foundation of Ministry of Education of China [2013201130004]
  3. Young National Natural Science Foundation of China [21202111]
  4. Young Natural Science Foundation of Jiangsu Province [BK2012174]
  5. Key Laboratory of Organic Synthesis of Jiangsu Province [KJS1211]
  6. PAPD
  7. Soochow University

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A novel and efficient protocol for the creation of 6-amino phenanthridine derivatives by Co(acac)(2)-catalyzed isocyanide insertion with 2-aryl anilines under an O-2 HAS atmosphere via homolytic aromatic substitution (HAS) type C-H ffinctionalization has been developed. This reaction not only proceeds smoothly utilizing O-2 as the oxidant but also provides a new approach to construct phenanthridine derivatives utilizing readily available 2-aryl anilines with isoc-yanides instead of 2-isocyanobiaryls with different radical precursors.

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