Etude de la cycloalcoylation des (thiényl-2)-5 pentènes-1

Cyclizations of 5(2-thienyl)pent-1-enes substituted at carbon-4 (COOH, COOCH 3 , CH 2 OH, or CH 3 ) by the action of mineral and Lewis acids are reported. The yield of cyclized product varies with the nature of the substituent, the acid catalyst employed, and the reaction time.

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Bibliographic Details
Published in:Canadian journal of chemistry 1970-08, Vol.48 (16), p.2587-2595
Main Authors: Gourier, J., Canonne, P.
Format: Article
Language:English
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Summary:Cyclizations of 5(2-thienyl)pent-1-enes substituted at carbon-4 (COOH, COOCH 3 , CH 2 OH, or CH 3 ) by the action of mineral and Lewis acids are reported. The yield of cyclized product varies with the nature of the substituent, the acid catalyst employed, and the reaction time.
ISSN:0008-4042
1480-3291
DOI:10.1139/v70-434