69903-57-7Relevant academic research and scientific papers
Preparation of (S)-γ-cyclogeraniol by lipase-catalyzed transesterification and synthesis of (+)-trixagol and (+)-luffarin-P
Fujii, Mikio,Morimoto, Yosuke,Ono, Machiko,Akita, Hiroyuki
, p. 160 - 166 (2015/12/04)
Lipase-catalyzed kinetic resolution of γ-cyclogeraniol by Candida antarctica lipase B yielded 23% of enantiomerically pure (S)-γ-cyclogeraniol. (+)-trixagol and (+)-luffarin-P were synthesized from the obtained (S)-γ-cyclogeraniol, and the absolute config
Synthesis of (+)-trixagol and its enantiomer, the terpenoid side chain of (-)-agelasine E
Bakkestuen, Anne Kristin,Gundersen, Lise-Lotte
, p. 115 - 121 (2007/10/03)
The naturally occurring γ-cyclogeranylgeraniol called (+)-trixagol has been synthesised for the first time. Trixagol was readily available in five steps from (S)-2,2-dimethyl-6-methylene-1-cyclohexanemethanol. The enantiomer of trixagol, which equates to
MINOR COMPONENTS WITH THE γ-CYCLOGERANIL GERANIOL SKELETON FROM BELLARDIA TRIXAGO (L.) ALL.
Pascual-T., J. De,Caballero, E.,Caballero, C.,Medarde, M.,Barrero, A. F.,Grande, M.
, p. 1837 - 1842 (2007/10/02)
Trixagol 1 and fourteen derivatives with the skeleton of γ-cyclogeranil geraniol were isolated from Bellardia trixago, the structures were determined by spectroscopic methods and confirmed by partial synthesis.Furthermore, 3,4-dihydro-γ-ionone, α-ambrinol
