Journal
TETRAHEDRON LETTERS
Volume 52, Issue 45, Pages 6015-6017Publisher
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
Categories
Funding
- Seoul RBD Program [PA100046M093212]
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available