Thienoquinolizidinones. Synthesis and rearrangement into new piperidino[1,2‐a][1,3] or [1,4]diazepinones fused to a thiophene ring
Identifieur interne : 001458 ( France/Analysis ); précédent : 001457; suivant : 001459Thienoquinolizidinones. Synthesis and rearrangement into new piperidino[1,2‐a][1,3] or [1,4]diazepinones fused to a thiophene ring
Auteurs : Stefan Marchalin [Tchécoslovaquie] ; Bernard Decroix [France]Source :
- Journal of Heterocyclic Chemistry [ 0022-152X ] ; 1994-03.
Abstract
A convenient route to thienoquinolizidinones is described starting from ethyl pipecolinate and suitable halogenomethylthiophenes or 3‐chloromethylbenzothiophene. The Schmidt reaction and the Beckmann rearrangement of oximes of these ketones led to piperidino[1,2‐a][1,3] or [1,4]diarepines fused to a thiophene ring.
Url:
DOI: 10.1002/jhet.5570310239
Affiliations:
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ISTEX:11EE0A1A83579EEAD37473FE28B0D7619582F63CLe document en format XML
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The Schmidt reaction and the Beckmann rearrangement of oximes of these ketones led to piperidino[1,2‐a][1,3] or [1,4]diarepines fused to a thiophene ring.</div></front></TEI><affiliations><list><country><li>France</li><li>Tchécoslovaquie</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="Tchécoslovaquie"><noRegion><name sortKey="Marchalin, Stefan" sort="Marchalin, Stefan" uniqKey="Marchalin S" first="Stefan" last="Marchalin">Stefan Marchalin</name></noRegion></country><country name="France"><region name="Région Normandie"><name sortKey="Decroix, Bernard" sort="Decroix, Bernard" uniqKey="Decroix B" first="Bernard" last="Decroix">Bernard Decroix</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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