250229-64-2Relevant academic research and scientific papers
Synthesis of (3S,7S)- and (3S,7S,15S)- stereoisomers of 3,7-dimethyl-2- heptacosanone and 3,7,15-trimethyl-2-heptacosanone, the ketones identified from the locust Schistocerca gregaria
Nakamura, Yoshihide,Mori, Kenji
, p. 1307 - 1312 (2007/10/03)
The (3S,7S) and (3S,7S,15S) stereoisomers of 3,7-dimethyl-2- heptacosanone (1) and 3,7,15-trimethyl-2-heptacosanone (2), the ketones identified from the locust Schistocerca gregaria, were synthesized by employing (2R,6S)-7-acetoxy-2,6-dimethyl-1-heptanol (4) as the starting material.
Pheromone synthesis, CXCVIII. Synthesis of (1S,2S,6S,10R)- and (1S,2R,6R,10R)-1,2,6,10-tetramethyldodecyl propanoate, the components of the sex pheromone of the pine sawfly, Microdiprion pallipes
Nakamura, Yoshihide,Mori, Kenji
, p. 2175 - 2182 (2007/10/03)
(1S,2S,6S,10R)- and (1S,2R,6R,10R)-1,2,6,10-tetramethyldodecyl propanoate (1 and 2), the components of the pheromone of Microdiprion pallipes, were synthesized from two chiral and nonracemic building blocks, (R)-3-tert-butoxycarbonyl-2-methylpropanoic acid (D) and (2R,6S)-7-acetoxy- 2,6-dimethyl-1-heptanol (G), by employing lipase-catalyzed kinetic resolution in a later step.
