Issue 3, 2022

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

Abstract

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
11 Nov 2021
Accepted
16 Dec 2021
First published
17 Dec 2021

Org. Biomol. Chem., 2022,20, 636-648

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

P. S. Dhote and C. V. Ramana, Org. Biomol. Chem., 2022, 20, 636 DOI: 10.1039/D1OB02207E

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