Stereoselective reduction of new fused azoninones with a bridgehead nitrogen
Identifieur interne : 001420 ( France/Analysis ); précédent : 001419; suivant : 001421Stereoselective reduction of new fused azoninones with a bridgehead nitrogen
Auteurs : Dusan Berkes [France] ; Nathalie Bar [France] ; Bernard Decroix [France]Source :
- Journal of Heterocyclic Chemistry [ 0022-152X ] ; 1995-03.
Abstract
The synthesis of methanothienoazoninones 5a,b is described starting from 2(3)‐halogenomethylthio‐phenes. Their reduction with sodium borohydride led to the corresponding aminoalcohols 6a,b with a complete stereoselectivity.
Url:
DOI: 10.1002/jhet.5570320205
Affiliations:
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Their reduction with sodium borohydride led to the corresponding aminoalcohols 6a,b with a complete stereoselectivity.</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="Berkes, Dusan" sort="Berkes, Dusan" uniqKey="Berkes D" first="Dusan" last="Berkes">Dusan Berkes</name></region><name sortKey="Bar, Nathalie" sort="Bar, Nathalie" uniqKey="Bar N" first="Nathalie" last="Bar">Nathalie Bar</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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