Kenji Mori, Ph.D.
Affiliations: | 1978- | University of Tokyo, Bunkyō-ku, Tōkyō-to, Japan |
Area:
Pheromone synthesisGoogle:
"Kenji Mori"Mean distance: 8.83
Children
Sign in to add traineeTakeshi Kitahara | grad student | ||
Hidenori Watanabe | grad student | ||
Narshinha P. Argade | post-doc | 1993-1994 |
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Publications
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Ohkubo Y, Akasaka K, Masuda Y, et al. (2020) Pheromone synthesis. Part 265: Synthesis and stereochemical composition of two pheromonal compounds of the female Korean apricot wasp, Eurytoma maslovskii Tetrahedron. 76: 131410 |
Mori K, Tabata J. (2017) Pheromone synthesis. Part 262: Determination of the absolute configuration of the female sex pheromone [(1 S ,2 S )-(−)-(1,2-dimethyl-3-methylenecyclopentyl) acetaldehyde] of the pineapple mealybug ( Dysmicoccus brevipes ) by synthesis coupled with X-ray analysis Tetrahedron. 73: 6530-6541 |
Szczerbowski D, Torrens GG, Rodrigues MACM, et al. (2016) (1R,6R)-2,2,6-Trimethyl-3-oxabicyclo[4.2.0]octan-4-one, a new monoterpene lactone produced by males of the cocoa borer Conotrachelus humeropictus (Col.: Curculionidae) Tetrahedron Letters. 57: 2842-2844 |
Sakai T, Matsushita S, Arakawa S, et al. (2015) Total Synthesis of Gymnocin-A. Journal of the American Chemical Society |
Mori N, Kitahara T, Mori K, et al. (2015) Asymmetric Formal Synthesis of Azadirachtin. Angewandte Chemie (International Ed. in English) |
Mori K, Miyake A, Akiyama T. (2015) Enantioselective synthesis of fused heterocycles with contiguous stereogenic centers by chiral phosphoric acid catalyzed symmetry breaking. Chemical Communications (Cambridge, England) |
Mori K, Akasaka K. (2015) Pheromone synthesis. Part 258. Synthesis of the enantiomers of the beetle pheromones ethyl 4-methylheptanoate, 4-methyloctanoic acid and 4-methyl-1-nonanol, and HPLC analysis of their derivatives to determine their enantiomeric purities Tetrahedron Asymmetry |
Mori K, Osada K, Amaike M. (2015) Mammalian blood odorant and chirality: synthesis and sensory evaluation by humans and mice of the racemate and enantiomers of trans-4,5-epoxy-(E)-2-decenal Tetrahedron Asymmetry. 26: 861-867 |
Mori K, Akasaka K. (2015) Pheromone synthesis. Part 256: Synthesis of the four stereoisomers of 5,11-dimethylpentacosane, a new sex pheromone component of the male Galleria mellonella (L.), with high stereochemical purities as determined by the derivatization-HPLC analysis of the eight stereoisomers of 5,11-dimethyl-8-pentacosanol Tetrahedron. 71: 4102-4115 |
Vuts J, Francke W, Mori K, et al. (2015) Pheromone Bouquet of the Dried Bean Beetle, Acanthoscelides obtectus (Col.: Chrysomelidae), Now Complete European Journal of Organic Chemistry. 2015: 4843-4846 |