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Terpenes and terpene derivatives-22

Tetrahedron, 1987
Abstract Isocanambrin ( 1 ) and 6-epi-isocordilin ( 21 ) were synthesized by twofold application of a reaction sequence starting from an α, β-unsaturated carbonyl compound via Wittig-Horner reaction , selective hydrogenation, epoxidation, and solvolysis to give a hydroxy-γ-lactone. Thus, aldehyde 4 was converted (→ 5 ,→ 8 ,→ 9
Peter Weyerstahl   +3 more
openaire   +1 more source

Terpenes

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Tilman Hahn   +2 more
openaire   +1 more source

Biotransformation of terpenes

Biotechnology Advances, 2006
The main application of terpenes as fragrances and flavors depends on the absolute configuration of the compounds because enantiomers present different organoleptic properties. Biotransformations allow the production of regio- and stereoselective compounds under mild conditions. These products may be labeled as "natural".
Carla C C R, de Carvalho   +1 more
openaire   +2 more sources

Terpene und terpen-derivate—vii

Tetrahedron, 1978
A. Hoppmann, P. Weyerstahl
openaire   +1 more source

Bacterial terpene cyclases

Natural Product Reports, 2016
This review summarises the characterised bacterial terpene cyclases and their products and discusses the enzyme mechanisms.
openaire   +2 more sources

Terpene

Fresenius' Zeitschrift für analytische Chemie, 1964
openaire   +2 more sources

Terpenes

2020
Andrew Pengelly, Kerry Bone
openaire   +2 more sources

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