Planta Med 2004; 70(7): 646-651
DOI: 10.1055/s-2004-827189
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

Conformational Analysis of the Biflavanoid GB2 and a Polyhydroxylated Flavanone-Chromone of Cratoxylum neriifolium

Vineet Kumar1 , 2 , Volker Brecht1 , August Wilhelm Frahm1
  • 1Department of Pharmaceutical Chemistry, 79104, Freiburg, Germany
  • 2Present address: Chemistry Division, Forest Research Institute, Dehra Dun - 248006, India
Further Information

Publication History

Received: December 1, 2003

Accepted: April 24, 2004

Publication Date:
15 July 2004 (online)

Abstract

Three compounds, namely the interesting biflavanonol GB-2 (naringenin I-3, II-8-dihydroquercetin, 1), I-4′,I-5,II-5,I-7,II-7-pentahydroxyflavanone(I-3,II-8)chromone [naringenin-(3→8) 5,7-dihydroxychromone, 2] and stigmasterol, have been isolated from the leaves of Cratoxylum neriifolium Kurz. Compounds 1 and 2 show rotameric behavior due to the presence of a single bond between the highly substituted flavanone and flavanonol part and the flavanone and chromone part, respectively. Complete NMR spectral assignments of 1 and 2 have been done at 27 °C and 90 °C for the first time followed by a study of conformational behavior at room temperature by ROESY.

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Prof. Dr. August Wilhelm Frahm

Department of Pharmaceutical Chemistry

Albertstr. 25

79104 Freiburg

Germany

Phone: +49-761-203-6334

Fax: +49-761-203-6351

Email: August.Wilhelm.Frahm@pharmazie.uni-freiburg.de

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