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Acid-catalyzed condensation of 2,2 '-diamino-1,1 '-biaryls for the synthesis of benzo[c]carbazoles
- Title
- Acid-catalyzed condensation of 2,2 '-diamino-1,1 '-biaryls for the synthesis of benzo[c]carbazoles
- Author
- 조천규
- Keywords
- 2,2′-Diamino-1,1′-biaryls; [3,3]-Sigmatropic rearrangement; Benzo[c]carbazole; Dibenzo[c,g]carbazole; Tandem reaction
- Issue Date
- 2011-09
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
- Citation
- TETRAHEDRON LETTERS, Vol.52, No.45 [2011], p6015-6017
- 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. ⓒ 2011 Elsevier Ltd. All rights reserved.
- URI
- https://www.sciencedirect.com/science/article/pii/S0040403911015115?via%3Dihubhttp://hdl.handle.net/20.500.11754/37460
- ISSN
- 0040-4039
- Appears in Collections:
- COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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