4.7 Article

Copper(II) Acetate/Oxygen-Mediated Nucleophilic Addition and Intramolecular C-H Activation/C-N or C-C Bond Formation: One-Pot Synthesis of Benzimidazoles or Quinazolines

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 352, Issue 17, Pages 2905-2912

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201000469

Keywords

carbodiimides; cascade reactions; C-H activation; copper(II) acetate catalysis; cyclization; one-pot reaction

Funding

  1. Natural Science Foundation of China [21072168]

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Diarylcarbodiimides or benzylphenylcarbodiimides are converted to 1,2-disubstituted benzimidazoles or 1,2-disustituted quinazolines via addition/intramolecular C-H bond activation/C-N or C-C bond forming reaction using copper(II) acetate/oxygen [Cu(OAc)(2)/O-2] as the oxidant at 100 degrees C in one-pot cascade procedure.

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