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Trivalent organophosphorus reagent induced pinacol rearrangement of 4H-cyclopenta[2,1-b:3,4-b′]dithiophen-4-one

Authors :
Marin, Lidia
Zhang, Yuexing
Robeyns, Koen
Champagne, Benoît
Adriaensens, Peter
Lutsen, Laurence
Vanderzande, Dirk
Bevk, David
Maes, Wouter
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Feb2013, Vol. 54 Issue 6, p526-529. 4p.
Publication Year :
2013

Abstract

Abstract: In this Letter we report on the reaction of 4H-cyclopenta[2,1-b:3,4-b′]dithiophen-4-one with various trivalent organophosphorus derivatives, with an emphasis on the final products depending on the applied reagents. No reaction occurred upon treatment with either triphenyl- or tricyclohexylphosphine, whereas addition of triethyl phosphite or tri(n-butyl)phosphine resulted in pinacol rearrangement. Structure elucidation of the isolated 5H-spiro(benzo[1,2-b:6,5-b′]dithiophene-4,4′-cyclopenta[2,1-b:3,4-b′]dithiophen)-5-one was achieved by combined NMR experiments, theoretical chemical shift and geometry calculations, and single crystal X-ray analysis. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
54
Issue :
6
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
84657139
Full Text :
https://doi.org/10.1016/j.tetlet.2012.11.068