Results 111 to 120 of about 51,986,713 (143)
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Inhalation of a racemic mixture (R,S)-linalool by rats experiencing restraint stress alters neuropeptide and MHC class I gene expression in the hypothalamus

Neuroscience Letters, 2017
Some odorants have physiological and psychological effects on organisms. However, little is known about the effects of inhaling them, particularly on the central nervous system. Using DNA microarray analysis, we obtained gene expression profiles of the hypothalamus from restraint stressed rats exposed to racemic (R,S)-linalool.
Kazushi, Yoshida   +5 more
openaire   +2 more sources

ChemInform Abstract: An Asymmetric Synthesis of Enantiomerically Pure (S)‐(+)‐Linalool (3,7‐Dimethyl‐1,6‐octadien‐3‐ol) and a Formal Synthesis of (R)‐(‐)‐Linolool.

ChemInform, 1987
AbstractSynthesis of S‐(+)‐linalool (VIII), using the optically active oxathiane (Ia) as a chiral template, is described.
M. OHWA, T. KOGURE, E. L. ELIEL
openaire   +1 more source

Characterisation of an (S)-linalool synthase from kiwifruit (Actinidia arguta) that catalyses the first committed step in the production of floral lilac compounds

Functional Plant Biology, 2010
Kiwifruit (Actinidia spp. Lindl.) flowers and fruit contain many compounds of interest to the flavour and fragrance industries. In particular, Actinidia arguta (Sieb. et Zucc.) Planch. ex Miq. flowers produce ß-linalool and important derivatives thereof, including linalool oxides, lilac aldehydes, alcohols and alcohol epoxides.
Xiuyin Chen   +7 more
openaire   +1 more source

Functional Characterization of a New Antarctic Microbial Esterase EST112-2 and Its Use in the Preparation of Chiral Tertiary Alcohol (S)-Linalool

Chinese Journal of Organic Chemistry, 2018
Chiral tertiary alcohols (TAs) are key building blocks for the synthesis of many crucial flavor compounds and pharmaceuticals. The two enantiomers of tertiary alcohol, linalool, differ in odor. So, sustainable strategies for the manufacture of optically pure TAs represented by linalool, are highly desirable.
Dun Deng   +4 more
openaire   +1 more source

Antimicrobial effect of vapours of terpineol, (R)‐(–)‐linalool, carvacrol, (S)‐(–)‐perillaldehyde and 1,8‐cineole on airborne microbes using a room diffuser

Flavour and Fragrance Journal, 2008
AbstractIn this study the antimicrobial activities of five volatiles, which represent main compounds of several essential oils, were tested. Terpineol, (R)‐(–)‐linalool, carvacrol, (S)‐(–)‐perillaldehyde and 1,8‐cineole were evaluated for their influence on airborne microbes when vaporized with a room diffuser.
Sabine Krist   +4 more
openaire   +1 more source

On the enantiomeric distribution of R(-) and S(+) linalool in Muscat Wine

2000
Linalool (3,7-dimethyl-1,6-octadien-3-ol)is one of the most characterizing flavour natural substances in muscati wine. This paper presents the results of the enantiomeric distribution of linalool in a typical product of the Portuguese market called "Moscatel Favaios" and produced by a technology similar to the Port wine one.
F. Tateo, M. Bononi, E. Lubian
openaire   +1 more source

Antimicrobial effect of vapours of terpineol, (R)-(-)-linalool, carvacrol, (S)-(-)-perillaldehyde and 1,8-cineole on airborne microbes using a room diffuser

Flavour & Fragrance Journal, 2008
ABSTRACT: In this study the antimicrobial activities of five volatiles, which represent main compounds of several essential oils, were tested. Terpineol, (R)-(¿)-linalool, carvacrol, (S)-(¿)-perillaldehyde and 1,8-cineole were evaluated for their influence on airborne microbes when vaporized with a room diffuser.
Krist, Sabine   +2 more
openaire   +1 more source

Integrative oncology: Addressing the global challenges of cancer prevention and treatment

Ca-A Cancer Journal for Clinicians, 2022
Jun J Mao,, Msce   +2 more
exaly  

Enantiospecific determination of the odour threshold concentrations of (R)- and (S)-linalool in water and beer

BrewingScience, 2023
Reglitz, Klaas   +7 more
openaire   +1 more source

High Pressure Densities and Derived Thermodynamic Properties of Pure (1R)-(+)-α-Pinene, (1S)-(−)-β-Pinene, and Linalool: Experiment and Modeling

Journal of Chemical & Engineering Data
Published as part of Journal of Chemical & Engineering Data virtual special issue “Proceedings of PPEPPD 2023”.
Nikola Grozdanić   +3 more
openaire   +2 more sources

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