112775-81-2Relevant academic research and scientific papers
SYNTHESIS AND BIOACTIVITY OF OPTICALLY ACTIVE FORMS OF 1-METHYL-2-CYCLOHEXEN-1-OL, AN AGGREGATION PHERONOME OF DENDROCTONUS PSEUDOTSUAGE
Mori, K.,Hazra, B. G.,Pfeiffer, R. J.,Gupta, A. K.,Lindgren, B. S.
, p. 2249 - 2254 (1987)
Both the enantiomers of 1-methyl-2-cyclohexen-ol, an aggregation pheromone of the female Douglas-fer beetle, were synthesized from the enantiomers of seudenol (3-methyl-2-cyclohexen-1-ol).The enantiomers were less active than the racemate of 1-methyl-2-cy
Pheromone Synthesis, CXI. - An Enzyme-Mediated Synthesis of Both Enantiomers of Seudenol and 1-Methyl-2-cyclohexen-1-ol, the Aggregation Pheromones of Dendroctonus pseudotsugae
Mori, Kenji,Ogoche, Jondiko I.J.
, p. 903 - 906 (2007/10/02)
Enzymatic resolution of seudenol acetate by pig liver esterase has led to an efficient preparation of both the enantiomers of seudenol and 1-methyl-2-cyclohexen-1-ol, the aggregation pheromones of the Douglas-fir beetle Dendroctonus pseudotsugae Hopkins.
