4.7 Article

Efficient synthesis of 2-arylquinazolin-4-amines via a copper-catalyzed diazidation and ring expansion cascade of 2-arylindoles

Journal

CHEMICAL COMMUNICATIONS
Volume 54, Issue 89, Pages 12602-12605

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc07721e

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Funding

  1. National Natural Science Foundation of China [21772138, 21672157]
  2. Project of Scientific and Technological Infrastructure of Suzhou [SZS201708]
  3. PAPD

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Copper-catalyzed synthesis of 2-arylquinazolin-4-amines from readily available 2-arylindoles and TMSN3 has been developed. The mechanism study shows that the domino reaction may involve a free radical diazidation, denitrogenation, intramolecular cyclization and ring expansion sequence.

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