First synthesis and Diels-Alder reaction of thieno[2,3(3,2)-f]indolizines
Identifieur interne : 001448 ( France/Analysis ); précédent : 001447; suivant : 001449First synthesis and Diels-Alder reaction of thieno[2,3(3,2)-f]indolizines
Auteurs : Abdelali Daich [France] ; Philippe Ohier [France] ; Bernard Decroix [France]Source :
- Tetrahedron Letters [ 0040-4039 ] ; 1994.
Abstract
Thieno[2,3(3,2)-f] indolizines were synthesized from 2-formyl-1-[thien-2(3)-ylmethyl]pymole. Under Diels-Alder reaction with diethyl acetylenedicarboxylate they led to cycl[3,2,2]azines fused to a thiophene ring.
Url:
DOI: 10.1016/0040-4039(94)02156-6
Affiliations:
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- to stream Istex, to step Curation: 000155
- to stream Istex, to step Checkpoint: 000F63
- to stream Main, to step Merge: 002190
- to stream Main, to step Curation: 002128
- to stream Main, to step Exploration: 002128
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<front><div type="abstract" xml:lang="en">Thieno[2,3(3,2)-f] indolizines were synthesized from 2-formyl-1-[thien-2(3)-ylmethyl]pymole. Under Diels-Alder reaction with diethyl acetylenedicarboxylate they led to cycl[3,2,2]azines fused to a thiophene ring.</div>
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