Results 231 to 240 of about 56,359 (272)
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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   +6 more
openaire   +1 more source

Synthetic Protein Scaffolds for Improving R-(-)-Linalool Production in Escherichia coli.

Journal of Agricultural and Food Chemistry, 2021
R-(-)-Linalool is widely used in the pharmaceutical, agrochemical, and fragrance industries; however, its applications are limited owing to low yield and high cost of production. To improve the production efficiency of R-(-)-linalool in Escherichia coli,
Jing Wu   +5 more
semanticscholar   +1 more source

Combinatorial Modulation of Linalool Synthase and Farnesyl Diphosphate Synthase for Linalool Overproduction in Saccharomyces cerevisiae.

Journal of Agricultural and Food Chemistry, 2021
Linalool, as a fragrant monoterpene, is an important feedstock for food, pharmaceuticals, and cosmetics industries. Although our previous study had significantly increased linalool production by the directed evolution of linalool synthase and ...
Pingping Zhou   +5 more
semanticscholar   +1 more source

Fragrance material review on linalool

Food and Chemical Toxicology, 2003
A toxicologic and dermatologic review of linalool when used as a fragrance ingredient, is presented.
C S, Letizia   +3 more
openaire   +2 more sources

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   +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   +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   +3 more
openaire   +2 more sources

Linalool: A ubiquitous floral volatile mediating the communication between plants and insects

, 2023
Ling Zhang   +5 more
semanticscholar   +1 more source

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   +3 more
openaire   +2 more sources

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