Total assignments of  1 H and  13 C NMR spectra of a new prenylated flavanone from  Dioclea grandiflora | Zendy

Lemos Virgínia S. | Zendy; dos Santos Marcelo H. | Zendy; Rabelo Luiza A. | Zendy; Côrtes Steyner F. | Zendy

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Total assignments of 1 H and 13 C NMR spectra of a new prenylated flavanone from Dioclea grandiflora

Author(s) -

Lemos Virgínia S.,

dos Santos Marcelo H.,

Rabelo Luiza A.,

Côrtes Steyner F.

Publication year - 2002

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.1096

Subject(s) - flavanone , chemistry , prenylation , fabaceae , stereochemistry , two dimensional nuclear magnetic resonance spectroscopy , nmr spectra database , carbon 13 nmr , spectral line , flavonoid , organic chemistry , botany , enzyme , physics , astronomy , biology , antioxidant

A new prenylated flavanone, floranol ( 1 ) 3,5,7,2′‐ tetrahydroxy‐6‐methoxy‐8‐prenylflavanone and a known flavanone (dioclein) were isolated from the roots of Dioclea grandiflora (Fabaceae). The structure and the relative stereochemistry were established by 2D NMR spectroscopic techniques (HMQC and HMBC) Copyright © 2002 John Wiley & Sons, Ltd.

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