z-logo
Premium
Determination of the absolute configuration of 6‐alkylated α‐pyrones from Ravensara crassifolia by LC‐NMR
Author(s) -
Queiroz E. F.,
Wolfender J.L.,
Raoelison G.,
Hostettmann K.
Publication year - 2003
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.684
Subject(s) - chemistry , absolute configuration , solvent , acetonitrile , proton nmr , deuterium , carbon 13 nmr , nmr spectra database , chromatography , analytical chemistry (journal) , spectral line , organic chemistry , physics , quantum mechanics , astronomy
Abstract The absolute configuration of asymmetric centres of two α‐pyrones isolated from Ravensara crassifolia was determined using the Mosher method. The conventional analysis of the purified ester derivatives by 1 H‐NMR was replaced by a rapid and sensitive method in which the α‐pyrones were analysed under isocratic reversed‐phase LC‐NMR conditions prior to and after derivatisation reactions. Comparison of the LC‐ 1 H‐NMR spectra of the actual α‐pyrones with those of the corresponding Mosher's esters recorded in the acetonitrile:deuterated water solvent system exhibited shifts comparable with those obtained using conventional deuterated solvents. Based on the shifts recorded, determination of the absolute configuration was possible by application of Mosher rules. The use of LC‐NMR has permitted a direct analysis of crude reaction mixtures containing less than 50 µg of the starting material. Completion of the reaction was checked by LC‐MS and the crude reaction mixture was analysed by stop‐flow LC‐NMR. This methodology seems very promising for the determination at the micro‐scale level of the absolute configuration of natural products which are available only in very small amounts. Copyright © 2003 John Wiley & Sons, Ltd.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here