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Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Behaviour of Thiophenes Substituted with Electron-Withdrawing Groups in Cycloaddition Reactions

Author(s): Claudia Della Rosa, Elisa Paredes, Maria Kneeteman and Pedro M.E. Mancini

Volume 1, Issue 4, 2004

Page: [369 - 371] Pages: 3

DOI: 10.2174/1570178043400695

Price: $65

Abstract

Substituted thiophenes can act as dienophiles in normal electron demand Diels-Alder reactions, nitro being one of the substituents. Cycloaddition with Danishefskys diene provides the benzothiophene derivatives with nitro side selectivity, α-substituted substrates being the more dienophilic. The reaction with isoprene leads mainly to the corresponding (pyrrol-1-yl)thiophenes.

Keywords: thiophenes, diels-alder, pyrroles, benzothiophenes


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