Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yasumasa Shikichi"'
Publikováno v:
Proceedings of the National Academy of Sciences. 111:3056-3061
Animals exhibit a spectacular array of traits to attract mates. Understanding the evolutionary origins of sexual features and preferences is a fundamental problem in evolutionary biology, and the mechanisms remain highly controversial. In some specie
Autor:
Joanne Y. Yew, Shigeyuki Tamogami, Kenji Mori, Yasumasa Shikichi, Kazuaki Akasaka, Shruti Shankar
Publikováno v:
Tetrahedron. 68:3750-3760
All the eight stereoisomers of 3-acetoxy-11,19-octacosadien-1-ol (1), the male sex pheromone (CH503) of Drosophila melanogaster, were synthesized from two acetylenic starting materials and the enantiomers of 3,4-epoxy-1-butanol PMB ether. Complete se
Publikováno v:
Tetrahedron. 66:7161-7168
The enantiomers of (11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol were synthesized from the enantiomers of 3,4-epoxy-1-butanol PMB ether. Its racemate was also synthesized. Its (S)-isomer and racemate were shown to possess the same pheromone activity as
Autor:
Yasumasa Shikichi, Kenji Mori
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 76:1419-1421
(1R,7Z)-1-Methyl-7-hexadecenyl acetate (1), the female sex pheromone of the honey locust gall midge (Dasineura gleditchiae), was synthesized from 6-hepten-1-ol in an 8.9% overall yield (eight steps). Hydrolytic kinetic resolution of (±)-1,2-epoxy-8-
Autor:
Kenji Mori, Yasumasa Shikichi
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 76:407-409
(R)-10-Methyl-2-tridecanone, the female sex pheromone of the southern corn rootworm (Diabrotica undecimpunctata howardi Barber), was synthesized in 9 steps from methyl (S)-3-hydroxy-2-methylpropanoate in a 15.7% overall yield. Olefin cross metathesis
Publikováno v:
Bioscience, biotechnology, and biochemistry. 77(9)
Eight analogues of (3R,11Z,19Z)-CH503 (3-acetoxy-11,19-octacosadien-1-ol), the anti-aphrodisiac pheromone of male Drosophila melanogaster, were synthesized for a bioassay. These were the enantiomers of 3-acetoxy-11,19-octacosadiyn-1-ol (1), 3-acetoxy
Autor:
Kenji Mori, Yasumasa Shikichi
Publikováno v:
Bioscience, biotechnology, and biochemistry. 76(10)
The enantiomers of citronellal were converted to all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, the female-produced sex pheromone components of the Lyclene dharma dharma moth. Three well-
Publikováno v:
Bioscience, Biotechnology & Biochemistry; Sep2013, Vol. 77 Issue 9, p1931-1938, 8p