(2R∗,3S∗,4S∗,2″R∗,3″S∗)-Guibourtinidol-(4α→8)-catechin, a biflavanoid procyanidin of the proguibourtinidin group from Senna macranthera: its relative stereochemistry and conformation-Reference-Cited by-同舟云学术

(2R∗,3S∗,4S∗,2″R∗,3″S∗)-Guibourtinidol-(4α→8)-catechin, a biflavanoid procyanidin of the proguibourtinidin group from Senna macranthera: its relative stereochemistry and conformation

Published:2015-03 Issue:5-6 Volume:26 Page:247-250
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Klika Karel D.,Ricarte Irvila,Trevisan Maria Teresa Salles,de Vasconcelos Silva Maria Goretti,Owen Robert W.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference25 articles.

1. Conformational equilibria in selected A-type trimeric procyanidins

2. Enantioselective synthesis of orthogonally protected (2R,3R)-(−)-epicatechin derivatives, key intermediates in the de novo chemical synthesis of (−)-epicatechin glucuronides and sulfates

3. Flavans and Proanthocyanidins;Porter,1994

4. The structure and synthesis of proguibourtinidins from Cassia abbreviata

5. A biflavanoid proanthocyanidin carboxylic acid and related biflavanoids from Acacia luederitzii Engl. var. retinens(Sim) J. Ross & Brenan

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