Results 211 to 220 of about 45,147 (258)

Biotransformation of linalool to furanoid and pyranoid linalool oxides by Aspergillus niger

Phytochemistry, 1998
Biotransformation of (+/-)-linalool with submerged shaking cultures of Aspergillus niger, particularly A. niger ATCC 9142, yielded a mixture of cis- and trans-furanoid linalool oxide (yield 15-24%) and cis- and trans-pyranoid linalool oxide (yield 5-9%).
J C, Demyttenaere, H M, Willemen
openaire   +2 more sources

Linalool and linalool oxide production in transgenic carnation flowers expressing the Clarkia breweri linalool synthase gene

Molecular Breeding, 2002
Most modern cut-flower cultivars, including those of carnation(Dianthus caryophyllus), lack distinct fragrance.Carnationcv. Eilat flowers produce and emit various fragrance compounds, includingbenzoic acid derivatives and sesquiterpenes, but not monoterpenes.
Michal Lavy, Amir Zuker, Efraim Lewinsohn, Olga Larkov, Uzi Ravid, Alexander Vainstein, David Weiss   +6 more
openaire   +1 more source

Linalool and linalool nerolidol synthases in roses, several genes for little scent

Plant Physiology and Biochemistry, 2018
Roses are widely appreciated for the appearance of their flowers and for their fragrance. This latter character results from the combination of different odorant molecules among which monoterpenes are often prevalent constituents. In this study, we report the cloning and characterization of three rose monoterpene synthases.
Magnard, JL, Bony, AR, Bettini, F, Campanaro, A, Blerot, B, Baudino, S, Jullien, F   +6 more
openaire   +4 more sources

Theoretical Investigation of Linalool Oxidation

The Journal of Physical Chemistry A, 2006
This study concerns the autoxidation of one of the most used fragrances in daily life, linalool (3,7-dimethyl-1,6-octadien-3-ol). It reacts with O2 to form hydroperoxides, which are known to be important contact allergens. Pathways for hydroperoxide formation are investigated by means of quantum mechanical electronic structure calculations.
Carina, Bäcktorp, J R Tobias Johnson, Wass, Itai, Panas, Maria, Sköld, Anna, Börje, Gunnar, Nyman   +5 more
openaire   +2 more sources

Enantioselective synthesis of each stereoisomer of the pyranoid linalool oxides: the linalool route

Tetrahedron: Asymmetry, 1999
Abstract Each of the four enantiomerically pure tetrahydropyran linalool oxides was prepared by separate enantioselective Sharpless dihydroxylation of (R)- or (S)-linalyl acetate with AD-mix-α or AD-mix-β, followed by a completely stereoselective N-phenylselenophthalimide cyclization of an intermediate allylic alcohol.
G. VIDARI, A. DI ROSA, G. ZANONI, BICCHI, Carlo   +3 more
openaire   +2 more sources

Isobaric (vapour+liquid) equilibria of (linalool+1-propanol) and (linalool+1-butanol)

The Journal of Chemical Thermodynamics, 2002
Abstract The isobaric (vapour + liquid) equilibria (VLE) data for (linalool + 1-propanol) and (linalool + 1-butanol) at the pressures p = (20.00, 30.00, 40.00, 50.00, and 60.00) kPa were measured using an inclined ebulliometer with a pump-like stirrer. The equilibrium liquid compositions were corrected by taking account of the effects of evaporation
Dongshun Deng, Haoran Li, Shijun Han
openaire   +1 more source

Fragrance material review on l-linalool

Food and Chemical Toxicology, 2008
A toxicologic and dermatologic review of l-linalool when used as a fragrance ingredient is presented.
A, Lapczynski, S P, Bhatia, C S, Letizia, A M, Api   +3 more
openaire   +2 more sources

Uncovering reasons for differential accumulation of linalool in tea cultivars with different leaf area

Food Chemistry, 2021
Lanting Zeng, Ziyin Yang
exaly  

Linalool

2022
openaire   +1 more source

Atmospheric oxidation of linalool

Naturwissenschaften, 1995
A. Calogirou, D. Kotzias, A. Kettrup
openaire   +1 more source