Synthesis of indolizidinediones annelated to a furan ring
Identifieur interne : 001C29 ( Main/Exploration ); précédent : 001C28; suivant : 001C30Synthesis of indolizidinediones annelated to a furan ring
Auteurs : Fridrich Szemes ; Štefan Marchalín ; Nathalie Bar [France] ; Bernard Decroix [France]Source :
- Journal of Heterocyclic Chemistry [ 0022-152X ] ; 1998-11.
Abstract
The furo[2,3(or 3,2)‐f]indolizidinediones 4a,b were synthesized in five steps from glutamic acid in good yield. The ketones were converted into trans alcohols 5a,b or oximes 6a,b (either as syn‐anti mixture or as single isomer). The selectivity of these reactions is discussed.
Url:
DOI: 10.1002/jhet.5570350625
Affiliations:
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The ketones were converted into trans alcohols 5a,b or oximes 6a,b (either as syn‐anti mixture or as single isomer). The selectivity of these reactions is discussed.</div></front></TEI><affiliations><list><country><li>France</li></country><region><li>Basse-Normandie</li><li>Haute-Normandie</li><li>Région Normandie</li></region><settlement><li>Caen</li><li>Le Havre</li></settlement><orgName><li>Université du Havre</li></orgName></list><tree><noCountry><name sortKey="Marchalin, Stefan" sort="Marchalin, Stefan" uniqKey="Marchalin S" first="Štefan" last="Marchalín">Štefan Marchalín</name><name sortKey="Szemes, Fridrich" sort="Szemes, Fridrich" uniqKey="Szemes F" first="Fridrich" last="Szemes">Fridrich Szemes</name></noCountry><country name="France"><region name="Région Normandie"><name sortKey="Bar, Nathalie" sort="Bar, Nathalie" uniqKey="Bar N" first="Nathalie" last="Bar">Nathalie Bar</name></region><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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