A Convenient Route To Polythiophenes
- 1 January 1984
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 14 (1) , 1-9
- https://doi.org/10.1080/00397918408060857
Abstract
The Michael addition of aldehydes to α,β-unsaturated ketones (or their Mannich base precursors) developed by Stetter1 has been applied to the synthesis of 1,4-diketones containing one or more thiophene rings. These diketones could be cyclized in high yields to terthienyls.Keywords
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