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Unité de recherche
COST
Numéro de projet
C05.0022
Titre du projet
Tools and Strategies for the Total Synthesis of Biologically Active Alkaloids: Transition Metal Mediated Synthesis Lythracea Alkaloids: (+)-Vertine
Titre du projet anglais
Tools and Strategies for the Total Synthesis of Biologically Active Alkaloids: Transition Metal Mediated Synthesis Lythracea Alkaloids: (+)-Vertine

Textes relatifs à ce projet

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Mots-clé
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Description succincte
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Partenaires et organisations internationales
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Résumé des résultats (Abstract)
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Références bases de données
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Textes saisis


CatégorieTexte
Mots-clé
(Anglais)
alkaloid synthesis; planar chirality; chromium
Programme de recherche
(Anglais)
COST-Action D28 - Natural Products as a Source for Discovery, Synthesis and Application of Pharmaceuticals
Description succincte
(Anglais)
Within a network dedicated to the synthesis of biologically active alkaloids, this project aims at the synthesis of (+)-Vertine. This natural product of the Lythracea alkaloid family plays a role in glucose level regulation in blood and lowers blood pressure; it is a sedative and has antiinflammatory properties. Vertine has not been synthesized previously. Its interesting pharmacological properties apart, the synthesis of the 13-membered lactone incorporating a Z alkene, a diaryl unit and a hydrophyridine is synthetically challenging and will present opportunities to develop and test new synthetic methods. Testing the biological activity of the target molecule and of some analogues will be possible within the network as well as via individual industrial collaborations.
Partenaires et organisations internationales
(Anglais)
BE, BG, CH, CY, CZ, DE, DK, ES, FI, FR, GR, HU, IE, IL, IS, IT, LV, NL, NO, RO, SE, SK, UK
Résumé des résultats (Abstract)
(Anglais)
(+)-Vertine is a member of the Lythracea alkaloid family with a number of interesting biological activities, notably glucose level regulation in blood and blood pressure reduction. Vertine has not been synthesized previously. Its interesting pharmacological properties apart, the synthesis of the 12-membered lactone incorporating a Z alkene, a diaryl unit and a hydropyridine is synthetically challenging. The question of an induced chiral axis of the biaryl unit by the other stereogenic elements in the constrained macrolactone molecule is intriguing.
Références bases de données
(Anglais)
Swiss Database: COST-DB of the State Secretariat for Education and Research Hallwylstrasse 4 CH-3003 Berne, Switzerland Tel. +41 31 322 74 82 Swiss Project-Number: C05.0022