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Original Articles

SCHWEFELVERBINDUNGEN DES ERDÖLS IX.1 CYCLOPENTATHIOPHENE AUS 3,5-DI(β-NAPHTHYL) −2,4-THIOPHENDI-CARBONSÄURE-DERIVATEN

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Pages 219-227 | Received 15 Mar 1985, Published online: 13 Dec 2006
 

Abstract

Ring closure reactions at the 3,5-di(β-naphthyl)-2,4-thiophenedicarboxylic acid and its derivates lead to the b- and c-anellated cyclopentathiophene systems 2, 3a and 3c. The angular structure of the ring closure products is proved by 1H-NMR-studies; UV/Vis-spectroscopic studies discriminate between the sides of anellation on the thiophene.

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