Issue 24, 1997

Synthesis of polyfunctionalized thiophenes and enediynes via ring-opening reactions of 3-lithiated thieno[2,3-b](and [3,2-b])thiophenes, 3,4-dilithiated thieno[2,3-b]thiophenes and 3,6-dilithiated thieno[3,2-b]thiophenes

Abstract

Solutions of the title lithiated thienothiophenes were synthesized from 2,5-disubstituted 3,4-dibromothieno[2,3-b]thiophenes or 3,6-dibromothieno[3,2-b]thiophenes via Br → Li exchange with 1.0 or 2.0 equiv. of BuLi (THF, –78 °C), respectively, and gave either polyfunctionalized thiophenes or polyfunctionalized enediynes (by a novel tandem ring-opening process in these cases) on being allowed to warm up to ambient temperature.

Article information

Article type
Paper

Chem. Commun., 1997, 2355-2356

Synthesis of polyfunctionalized thiophenes and enediynes via ring-opening reactions of 3-lithiated thieno[2,3-b](and [3,2-b])thiophenes, 3,4-dilithiated thieno[2,3-b]thiophenes and 3,6-dilithiated thieno[3,2-b]thiophenes

L. S. Fuller, B. Iddon MP and K. A. Smith, Chem. Commun., 1997, 2355 DOI: 10.1039/A707033K

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