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

Authors
Lim, Byong-YunChoi, Min-KyungCho, Cheon-Gyu
Issue Date
Nov-2011
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
2,2 ' -Diamino-1,1 ' -biaryls; Benzo[c]carbazole; Dibenzo[c,g]carbazole; [3,3]-Sigmatropic rearrangement; Tandem reaction
Citation
TETRAHEDRON LETTERS, v.52, no.45, pp.6015 - 6017
Indexed
SCIE
SCOPUS
Journal Title
TETRAHEDRON LETTERS
Volume
52
Number
45
Start Page
6015
End Page
6017
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/144824
DOI
10.1016/j.tetlet.2011.09.001
ISSN
0040-4039
Abstract
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.
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