Synthesis of modified proanthocyanidins: introduction of acyl substituents at C-8 of catechin. Selective synthesis of a C-4 → O → C-3 ether-linked procyanidin-like dimer
- Author
- BEAUHAIRE, Josiane1 ; NOUR-EDDINE ES-SAFI1 2 ; BOYER, Francois-Didier1 ; KERHOAS, Lucien1 ; LE GUERNEVE, Christine3 ; DUCROT, Paul-Henri1
[1] Unité de Phytopharmacie et Médiateurs Chimiques, Inra, Route de Saint-Cyr, 78026 Versailles, France
[2] Laboratoire de Chimie Organique et d'Études Physico-chimiques, École Normale Supérieure, B.P. 5118, Takaddoum Rabat, Morocco
[3] UMR Sciences pour l'Œnologie, Inra, 2, place Viala, 34060 Montpellier, France - Source
Bioorganic & medicinal chemistry letters (Print). 2005, Vol 15, Num 3, pp 559-562, 4 p
- ISSN
- 0960-894X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Catéchine Dimère Ether Flavonoïde Oligomère Polyphénol Proanthocyanidine Réaction catalytique Régiosélectivité Synthèse chimique Sélectivité Tanin Titane IV Chlorure Procyanidine
- Keyword (en)
- Catechin Dimer Ether Flavonoid Oligomer Polyphenol Proanthocyanidin Catalytic reaction Regioselectivity Chemical synthesis Selectivity Tannin Titanium IV Chlorides
- Keyword (es)
- Catequina Dímero Eter Flavonoide Oligómero Polifenol Proantocianidina Reacción catalítica Regioselectividad Síntesis química Selectividad Tanino Titanio IV Cloruro
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16478177
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.bmcl.2004.11.046 
https://dx.doi.org/10.1016/j.bmcl.2004.11.046
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