Synthesis and reactivity of oxopyrrolidinothieno[2]azepinones: [3]Benzazepine antidepressant analogs
Identifieur interne : 001362 ( France/Analysis ); précédent : 001361; suivant : 001363Synthesis and reactivity of oxopyrrolidinothieno[2]azepinones: [3]Benzazepine antidepressant analogs
Auteurs : Aïcha Mamouni [France] ; Adam Daïch [France] ; Bernard Decroix [France]Source :
- Journal of Heterocyclic Chemistry [ 0022-152X ] ; 1996-07.
Abstract
A synthesis of oxopyrrolidino[2]azepinones annelated to a thiophene ring 3a,b,c is described starting from succinimide and halogenomethylthiophenes 6a,b,c. Stereoselective reduction, Schmidt reaction and the Beckmann rearrangement of the oximes of the ketones 3a,b,c are studied.
Url:
DOI: 10.1002/jhet.5570330443
Affiliations:
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annelated to a thiophene ring 3a,b,c is described starting from succinimide and halogenomethylthiophenes 6a,b,c. Stereoselective reduction, Schmidt reaction and the Beckmann rearrangement of the oximes of the ketones 3a,b,c are studied.</div></front></TEI><affiliations><list><country><li>France</li></country><region><li>Haute-Normandie</li><li>Région Normandie</li></region><settlement><li>Le Havre</li></settlement><orgName><li>Université du Havre</li></orgName></list><tree><country name="France"><region name="Région Normandie"><name sortKey="Mamouni, Aicha" sort="Mamouni, Aicha" uniqKey="Mamouni A" first="Aïcha" last="Mamouni">Aïcha Mamouni</name></region><name sortKey="Daich, Adam" sort="Daich, Adam" uniqKey="Daich A" first="Adam" last="Daïch">Adam Daïch</name><name sortKey="Decroix, Bernard" sort="Decroix, Bernard" uniqKey="Decroix B" first="Bernard" last="Decroix">Bernard Decroix</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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