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Enantiomeric differentiation of bornyl acetate by 13 C‐NMR using a chiral lanthanide shift reagent
Author(s) -
Baldovini Nicolas,
Tomi Félix,
Casanova Joseph
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.710
Subject(s) - chemistry , lanthanide , reagent , enantiomer , enantiomeric excess , organic chemistry , carbon 13 nmr , enantioselective synthesis , catalysis , ion
The enantiomeric differentiation of bornyl acetate was carried out by 13 C‐NMR spectroscopy using a chiral lanthanide shift reagent. The technique was successfully applied to the determination of the enantiomer of bornyl acetate present in the essential oil of Inula graveolens . Copyright © 2003 John Wiley & Sons, Ltd.
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