Results 161 to 170 of about 3,753 (208)

Thienyl analogues of acyclic monoterpene alcohols and their biological activity

Journal of the Science of Food and Agriculture, 2009
AbstractBACKGROUND: Thienyl analogues of linalool, geraniol, nerol and citronellol were synthesised and their sensory and anti‐ microbial activities were investigated.RESULTS: The thienyl analogues of linalool, geraniol, nerol and citronellol, in which the isobutenyl moiety was replaced by a thiophene substituent, were synthesised from commercially ...
Radosław Bonikowski, Magdalena Sikora, Józef Kula, Alina Kunicka   +3 more
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Acyclic monoterpene primary alcohol:NADP+ oxidoreductase of Rauwolfia serpentina cells: the key enzyme in biosynthesis of monoterpene alcohols.

Journal of biochemistry, 1991
Acyclic monoterpene primary alcohol:NADP+ oxidoreductase, a key enzyme in the biosynthesis of monoterpene alcohols in plants, is unstable and has been only poorly characterized. However we have established conditions which stabilize the enzyme from Rauwolfia serpentina cells, and then purified it to homogeneity.
H, Ikeda, N, Esaki, S, Nakai, K, Hashimoto, S, Uesato, K, Soda, T, Fujita   +6 more
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ChemInform Abstract: ACYCLIC POLYHALOGENATED MONOTERPENES FROM THE RED ALGAE PLOCAMIUM VIOLACEUM

Chemischer Informationsdienst, 1977
AbstractDie halogenierten Diene (I) und (II) werden aus Algen isoliert und ihre Strukturen anhand von bekannten ähnlichen Verbindungen sichergestellt.
P. CREWS, E. KHO‐WISEMAN
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ChemInform Abstract: Anatoliosides: Five Novel Acyclic Monoterpene Glycosides from Viburnum orientale.

ChemInform, 1993
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
I. CAHS, A. YUERUEKER, H. RUEEGGER, A. D. WRIGHT, O. STICHER   +4 more
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Anatoliosides: Five Novel Acyclic Monoterpene Glylcosides from Viburnum orientale

Helvetica Chimica Acta, 1993
AbstractFive new acyclic monoterpene glycosides 1–5 were isolated from the leaves of Viburnum orientale (Caprifoliaceae). Anatolioside (1) is a monoterpene diglycoside and its structure was elucidated as linalo‐6‐yl 2′‐O‐(α‐L‐rhamnopyranosyl)β‐D‐glucopyranoside (arbitrary numbering of linalool moiety). Compounds 2–5 are all derivatives of 1, containing
Ihsan Çaliş, Ayşen Yürüker, Heinz Rüegger, Anthony D. Wright, Otto Sticher   +4 more
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Metabolism of structurally modified acyclic monoterpenes by Pseudomonas incognita

Canadian Journal of Microbiology, 1984
The ability of Pseudomonas incognita to metabolize some structurally modified acyclic monoterpenes was tested. The 6,7 double bond was found essential for these compounds to serve as a substrate for this organism, whereas the same was not true with the 1,2 double bond.
Renganathan, V, Madhava Madyastha, K
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A new acyclic monoterpene glucoside from the capitula of Tagetes patula

Fitoterapia, 1999
Abstract A new acyclic monoterpene glucoside, 2-methyl-6-methylen-2,7-octadiene-1- O -β- d -glucopyranoside (1) was isolated from Tagetes patula flowers in addition to known compounds helenien, xanthophyll, patuletin and patuletrin.
S.N. Garg, Reena Charles, Sushil Kumar
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Anatolioside E: A New Acyclic Monoterpene Glycoside from Viburnum orientale

Helvetica Chimica Acta, 1993
AbstractA new open‐chain monoterpene glycoside, anatolioside E (1), was isolated from the leaves of Viburnum orientale in addition to three known acyclic monoterpene glycosides, betulalbusides A (2) and B (3), and 2(E)‐2,6‐dimethyl‐2,7‐octadien‐1,6‐diol‐6‐O‐β‐D‐glucopyranoside(4).
Ihsan Çaliş, Ayşen Yürüker, Heinz Rüegger, Anthony D. Wright, Otto Sticher   +4 more
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ChemInform Abstract: Anatolioside E: A New Acyclic Monoterpene Glycoside from Viburnum orientale.

ChemInform, 1994
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
I. CALIS, A. YUERUEKER, H. RUEEGGER, A. D. WRIGHT, O. STICHER   +4 more
openaire   +1 more source

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

Journal of Environmental Science and Health, Part A, 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 ...
Yasutaka, Shimotori, Kazuyuki, Hattori, Masakazu, Aoyama, Tetsuo, Miyakoshi   +3 more
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