Microbiologically-assisted hemisynthesis of 1a-hydroxydrimenol

Gérard Aranda 1 M. Cortés 2 M. Maurs 3 R. Azerad 3
1 DCSO - Laboratoire de synthèse organique
2 Pontificia Universidad Católica de Chile
3 LCBPT - UMR 8601 - Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques
Abstract : The hemisynthesis of 1a-hydroxydrimenol has been selected to illustrate a synthetic route involving an initial microbial 3ß-hydroxylation of a drimenol derivative followed by a functionalization transfer to position 1a, thus generating a new potentially bioactive hydroxylated terpenic compound. Several methods have been investigated for the protection and the regeneration of the 7,8-double bond of drimenyl derivatives. © 2001 Elsevier Science Ltd. All rights reserved.
Type de document :
Article dans une revue
Tetrahedron: Asymmetry, Elsevier, 2001, 12 (14), pp.2013-2018. 〈10.1016/s0957-4166(01)00353-6〉
Liste complète des métadonnées
https://hal-polytechnique.archives-ouvertes.fr/hal-00954877
Contributeur : Denis Roura <>
Soumis le : mercredi 12 mars 2014 - 21:49:48
Dernière modification le : jeudi 10 mai 2018 - 02:07:51

Lien texte intégral

istex

Identifiants

Collections

X-DCSO | X | PARISTECH | UNIV-PARIS5 | INC-CNRS | USPC | X-DEP-CHIM

Citation

Gérard Aranda, M. Cortés, M. Maurs, R. Azerad. Microbiologically-assisted hemisynthesis of 1a-hydroxydrimenol. Tetrahedron: Asymmetry, Elsevier, 2001, 12 (14), pp.2013-2018. 〈10.1016/s0957-4166(01)00353-6〉. 〈hal-00954877〉

Exporter

BibTeX TEI DC DCterms EndNote

Partager

Métriques

Consultations de la notice

93

Contact

support.ccsd.cnrs.fr
hal.support@ccsd.cnrs.fr
Logo CCSD