Results 81 to 90 of about 41,423,758 (122)

An asymmetric synthesis of enantiomerically pure (S)-(+)-linalool (3,7-dimethyl-1,6-octadien-3-ol) and a formal synthesis of (R)-(-)-linalool

The Journal of Organic Chemistry, 1986
Masaki Ohwa, Tetsuo Kogure, Ernest L. Eliel   +2 more
openaire   +2 more sources

Densities, Viscosities, and Excess Molar Enthalpies of Binary Mixtures Containing Essential Oils at (298.15 and 313.15) K. The (S)-(−)-Limonene + Cineole, (S)-(−)-Limonene + Linalool, and Cineole + Linalool Systems

Journal of Chemical & Engineering Data, 2001
Densities, ρ, viscosities, η, and excess molar enthalpies, , of binary mixtures containing (S)-(−)-limonene [(−)-1-methyl-4-(1-methylethenyl)cyclohexene] + 1,8-cineole (1,3,3-trimethyl-2-oxabicyclo[2,2,2]octane), (S)-(−)-limonene + linalool (3,7-dimethyl-1,6-octadien-3-ol), and cineole + linalool were determined at (298.15 and 313.15) K and at ...
Fabio Comelli, Romolo Francesconi, Carlo Castellari   +2 more
openaire   +1 more source

Linalool attenuates lipid accumulation and oxidative stress in metabolic dysfunction-associated steatotic liver disease via Sirt1/Akt/PPRA-α/AMPK and Nrf-2/HO-1 signaling pathways.

Clinics And Research in Hepatology and Gastroenterology, 2023
INTRODUCTION Linalool is a monoterpene that occurs naturally in various aromatic plants and is identified in our previous study as a potential candidate for protection against high-fat diet (HFD)-induced metabolic dysfunction-associated steatotic liver ...
P. Tamilmani, V. S. Sathibabu Uddandrao, P. Chandrasekaran, G. Saravanan, P. Brahmanaidu, S. Sengottuvelu, S. Vadivukkarasi   +6 more
semanticscholar   +1 more source

Two-step enzymatic resolution process for large-scale production of (R)- and (S)-linalool

Bioresource Technology
Optically pure linalool with (R)- and (S)-configurations is a pivotal chiral building block in the flavors and fragrances industry as well as in sustainable crop protection. However, current production of (R)- and (S)-linalool relies on plant extraction, which is severely restricted by the spatiotemporal differences in enantiomer distribution, leading ...
Xun Wang, Xiaolong Kong, Weisheng Wang, Ziwei Jing, Fei Wang, Zhiguo Wang, Xun Li   +6 more
openaire   +2 more sources

Computational Molecular Docking Analysis of Linalool Enantiomers Interaction With Mitogen-Activated Protein Kinase 1 (MAPK1): Insights Into Potential Binding Mechanisms and Affinity.

Chirality
Molecular docking analysis of linalool interaction with mitogen-activated protein kinase 1 (MAPK1) provides valuable insights into the potential binding mechanisms and affinity of this interaction.
Halima Oulad Ali, N. Belboukhari, K. Sekkoum, Mebarka Belboukhari, L. Seddiki   +4 more
semanticscholar   +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

Inhibitory effect of thyme and basil essential oils, carvacrol, thymol, estragol, linalool and p-cymene towards Shigella sonnei and S. flexneri

Food Microbiology, 2004
There are a few reports on the antimicrobial activity of essential oils or their major constituents towards Shigella sp. The antimicrobial effect of basil and thyme essential oil and its major constituents thymol, p-cymene, estragol, linalool, and carvacrol was determined using the agar well diffusion assay. Thyme essential oil and thymol and carvacrol
C.F Bagamboula, M Uyttendaele, J Debevere   +2 more
openaire   +1 more source

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

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, Kei Sato, Sabine Glasl, Martina Hoeferl, Johannes Saukel   +4 more
openaire   +1 more source

Unraveling the Enantiomeric Distribution of Glycosidically Bound Linalool in Teas (Camellia sinensis) and Their Acidolysis Characteristics and Pyrolysis Mechanism.

Journal of Agricultural and Food Chemistry
Glycosidically bound linalool plays important roles in the formation of excellent tea flavor, while their enantiomeric distribution in teas and the actual transformations with free linalool are still unclear.
Han Yan, Zhi Lin, Weixuan Li, Jian-Jian Gao, Peng-Liang Li, Qin-Cao Chen, Hai-Peng Lv, Yue Zhang, Wei-Dong Dai, Zhi Lin, Yin Zhu   +10 more
semanticscholar   +1 more source