4.8 Article

Cu-Catalyzed Denitrogenative Ring-Opening of 3-Aminoindazoles for the Synthesis of Aromatic Nitrile-Containing (Hetero)Arenes

Journal

ORGANIC LETTERS
Volume 20, Issue 19, Pages 6161-6165

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b02629

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Funding

  1. Recruitment Program of Global Experts (1000 Talents Plan)
  2. Natural Science Foundation of Fujian Province [2016J01064]
  3. Fujian Hundred Talents Plan
  4. Program of Innovative Research Team of Huaqiao University [Z14X0047]
  5. Subsidized Project for Cultivating Postgraduates' Innovative Ability in Scientific Research of Huaqiao University

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An unprecedented Cu-catalyzed oxidative cleavage of two C-N bonds of 3-aminoindazoles is reported herein, which represents the first example for denitrogenative ring-opening of 3-aminoindazoles. This novel reactivity of 3-aminoindazoles enables the production of diverse aromatic nitrile-containing (hetero)arenes via C-H arylation of (hetero)-arenes with wide subsrate scope under mild conditions.

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