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Determination of the enantiomeric composition of (+)‐terpinen‐4‐ol from sweet marjoram Origanum majorana L. using a chiral lanthanide shift reagent
Year:
1987
Source of publication :
Flavour and Fragrance Journal
Authors :
Bassat, Michal
;
.
Putievsky, Eli
;
.
Ravid, Uzi
;
.
Volume :
2
Co-Authors:
Ravid, U., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Bassat, M., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Putievsky, E., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Ikan, R., Department of Organic Chemistry, Natural Products Laboratory, Hebrew University of Jerusalem, Jerusalem, 91-904, Israel
Weinstein, V., Department of Organic Chemistry, Natural Products Laboratory, Hebrew University of Jerusalem, Jerusalem, 91-904, Israel
Facilitators :
From page:
17
To page:
19
(
Total pages:
3
)
Abstract:
1H‐NMR examination of (+)‐terpinen‐4‐ol, performed in the presence of various molar ratios of a chiral lanthanide shift reagent Eu(hfc)3, showed that the enantiomeric composition of (+)‐terpinen‐4‐ol isolated from the essential oil of sweet marjoram is 73%(+): 27%(−). Peak assignment of the enantiomers was achieved by spiking the natural (+)‐enantiomer with the commercial (−)‐alcohol. The method will readily reveal adulteration of natural oils with racemic synthetics. Copyright © 1987 John Wiley & Sons, Ltd
Note:
Related Files :
1H‐NMR
(+)‐Terpinen‐4‐ol
Chiral Eu(hfc)3
Enantiomeric composition
Origanum majorana L
Sweet marjoram
Show More
Related Content
More details
DOI :
10.1002/ffj.2730020104
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
27721
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:33
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Scientific Publication
Determination of the enantiomeric composition of (+)‐terpinen‐4‐ol from sweet marjoram Origanum majorana L. using a chiral lanthanide shift reagent
2
Ravid, U., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Bassat, M., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Putievsky, E., Department of Medicinal, Spice and Aromatic Plants, Agricultural Research Organization, Newe Ya'ar, Post, Haifa, 31-999, Israel
Ikan, R., Department of Organic Chemistry, Natural Products Laboratory, Hebrew University of Jerusalem, Jerusalem, 91-904, Israel
Weinstein, V., Department of Organic Chemistry, Natural Products Laboratory, Hebrew University of Jerusalem, Jerusalem, 91-904, Israel
Determination of the enantiomeric composition of (+)‐terpinen‐4‐ol from sweet marjoram Origanum majorana L. using a chiral lanthanide shift reagent
1H‐NMR examination of (+)‐terpinen‐4‐ol, performed in the presence of various molar ratios of a chiral lanthanide shift reagent Eu(hfc)3, showed that the enantiomeric composition of (+)‐terpinen‐4‐ol isolated from the essential oil of sweet marjoram is 73%(+): 27%(−). Peak assignment of the enantiomers was achieved by spiking the natural (+)‐enantiomer with the commercial (−)‐alcohol. The method will readily reveal adulteration of natural oils with racemic synthetics. Copyright © 1987 John Wiley & Sons, Ltd
Scientific Publication
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