Results 111 to 120 of about 78,928 (170)

Chemical Composition and Biological Activities of Diverse Products from <i>Commiphora gileadensis</i>: A Comparative Review. [PDF]

Pharmaceuticals (Basel)
Alanazi FK, Hashad N, Ahmed AA, Ibrahim HA, Ibrahim RR, Abdelhady MIS, Haggag EG, Abdel Bar FM.   +7 more
europepmc   +1 more source

<i>Mentha</i> Essential Oils: Unraveling Chemotype-Dependent Biosynthesis and Assessing Evidence for Health-Promoting Activities. [PDF]

Nutrients
Yu Y, Ma Y, Ouyang Z, Huang L.
europepmc   +1 more source

Volatile Compounds Profiling of Fresh <i>R. alba</i> L. Blossom by Headspace-Solid Phase Microextraction and Gas Chromatography. [PDF]

Molecules
Antonova-Nedeltcheva D, Dobreva A, Gechovska K, Antonov L.   +3 more
europepmc   +1 more source

Multidimensional analysis of floral scent emission patterns in Phalaenopsis 'Chanel'. [PDF]

BMC Plant Biol
Ding L, Xu L, Feng K, Ruan J, Wu L, Yang C, Yu R.   +6 more
europepmc   +1 more source

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Microbial transformations of acyclic monoterpenes

Proceedings of the Indian Academy of Sciences - Section A, 1984
Microbial degradation of geraniol, citronellol, linalool and their corresponding acetates, structurally modified linalool and linalyl acetate, α-terpineol and β-myrcene are presented. Oxygenative and prototropic rearrangements are normally observed during the microbial metabolism of monoterpenes.
K Madhava Madyastha
exaly   +3 more sources

Bioefficacy of acyclic monoterpenes and their saturated derivatives against the West Nile vector Culex pipiens

Chemosphere, 2014
Twenty acyclic monoterpenes with different functional groups (acetoxy, hydroxyl, carbonyl and carboxyl) bearing a variable number of carbon double bonds were assayed as repellent and larvicidal agents against the West Nile vector Culex pipiens. Seven of them were derivatives that were synthesized through either hydrogenation or oxidation procedures ...
Veroniki P Vidali, Dimitrios Papachristos, Antonios Michaelakis   +2 more
exaly   +4 more sources

Acyclic monoterpenes in tree essential oils as a shrinking agent for waste-expanded polystyrene

Journal of Environmental Science and Health - Part A Toxic/Hazardous Substances and Environmental Engineering, 2011
We examined the dissolution of polystyrene (PS) into acyclic monoterpenes present in tree essential oils, to develop an environmentally friendly shrinking agent for waste-expanded polystyrene (EPS). The dissolving powers of geranyl acetate, geranylacetone, and geranyl formate [221.8-241.2 g PS (100 g solvent)(-1)] compared favorably with that of (R ...
Tetsuo Miyakoshi, Yasutaka Shimotori, Kazuyuki Hattori   +2 more
exaly   +4 more sources

Acyclic monoterpenes from the essential oil of Tagetes minuta flowers

Phytochemistry, 1998
Abstract The steam-distilled essential oil of T. minuta flowers afforded three new acylic monoterpene ketones identified as 3,7-dimethyloct-1-en-6-one, 3,7-dimethyl-5-hydroxyoct-1-en-6-one and 3,7-dimethyloct-1,7-dien-6-one along with major compounds ( Z )- β -ocimene (38.77%), dihydrotagetone (9.07%), ( Z )-tagetone (7%), ( Z )-ocimenone and ( E )-
S. Garg, V. K. Mehta
exaly   +4 more sources

Facile functionalization of the isopropylidene terminus of acyclic monoterpenes by way of benzenesulfenyl chloride addition

Tetrahedron, 1984
Abstract Highly site- and regioselective terminal functionalizations of acyclic monoterpenes 1 via benzenesulfenyl chloride addition followed by hydrolysis assisted by silica gel, dehydrochlorination under neutral or weakly basic condition, or dehydrochlorination by strongly basic treatment respectively providing β-hydroxy sulfides 3, terminal ...
Yukio Masaki, Kenji Kaji
exaly   +3 more sources