4.6 Article

Rediscovering Bacon's hydrazine/phenylhydrazine mediated cyclization of 2,2′-dicarbonylbi(hetero)aryls: construction of (5-azo)-/indazolo[2,3-a]quinolines

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 20, Issue 3, Pages 636-648

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob02207e

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Funding

  1. SERB
  2. DST-INSPIRE

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The hydrazine/phenylhydrazine-mediated reductive dicarbonyl coupling reactions have been successfully carried out under mild conditions, providing polycyclic aromatic compounds and azo-substituted polyaromatic compounds with a broad substrate scope and good functional group compatibility.
Hydrazine/phenylhydrazine-mediated reductive dicarbonyl coupling reactions have been carried out under mild conditions to provide polycyclic aromatic compounds and azo-substituted polyaromatic compounds. This method has a broad substrate scope with good functional group compatibility.

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