4.4 Article

Acid-catalyzed condensation of 2,2′-diamino-1,1′-biaryls for the synthesis of benzo[c]carbazoles

Journal

TETRAHEDRON LETTERS
Volume 52, Issue 45, Pages 6015-6017

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.09.001

Keywords

2,2 '-Diamino-1,1 '-biaryls; Benzo[c]carbazole; Dibenzo[c,g]carbazole; [3,3]-Sigmatropic rearrangement; Tandem reaction

Funding

  1. Seoul RBD Program [PA100046M093212]

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2,2'-Diamino-1,1'-biaryls were found to undergo ring-closure condensation reaction to afford benzo[c]carbazoles in good to excellent yield. Coupled with the synthesis of 2,2'-biaryldiamines from diaryl hydrazides via [3,3]-sigmatropic rearrangement, it constitutes a new efficient synthetic method for benzo[c]carbazoles and related compounds. (C) 2011 Elsevier Ltd. All rights reserved.

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