Short Enantioselective Syntheses of trans-5-Alkylprolines from New Functionalized Amino Alcohols

Jeanne Alladoum; Sylvain Roland; Emmanuel Vrancken; Pierre Mangeney; Catherine Kadouri-Puchot

doi:10.1021/jo8014243

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Short Enantioselective Syntheses of trans-5-Alkylprolines from New Functionalized Amino Alcohols

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Short Enantioselective Syntheses of trans-5-Alkylprolines from New Functionalized Amino Alcohols

Jeanne Alladoum, Sylvain Roland, Emmanuel Vrancken, Pierre Mangeney et Catherine Kadouri-Puchot

Journal of organic chemistry, Vol.2008(73), pp.9171-9774

19/12/2008

DOI: https://doi.org/10.1021/jo8014243

PMID: 18834177

Résumé

Chemical Sciences

Organic chemistry

Amino alcohols, having an enol ether function, cyclized in acidic medium to give quantitatively diastereosomerically pure bicyclic compounds that were transformed in five steps in enantiopure trans-5-alkylproline derivatives.

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Détails

Titre: Short Enantioselective Syntheses of trans-5-Alkylprolines from New Functionalized Amino Alcohols
Créateurs - sans rôle: Jeanne Alladoum - Chimie Organique
Sylvain Roland - Chimie Organique
Emmanuel Vrancken - Chimie Organique
Pierre Mangeney - Chimie Organique
Catherine Kadouri-Puchot - Chimie Organique
Détails de publication: Journal of organic chemistry, Vol.2008(73), pp.9171-9774
Éditeur: American Chemical Society
Nombre de pages: 604
Identifiants: 99138834109311
Unité académique: Institut Charles Gerhardt Montpellier - ICGM
Langue: English
Type de ressource: Journal article