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Volumn 87, Issue 1, 1999, Pages 103-104

Lipase-catalyzed kinetic resolution of 2,3-epoxy-1-tridecanol and its application to facile synthesis of (+)-disparlure

Author keywords

Disparlure; Gypsy moth; Lipase; Sex pheromones; Synthesis

Indexed keywords

ACYLATION; BIOSYNTHESIS; CATALYSIS; ENZYME KINETICS; HORMONES; SUBSTRATES;

EID: 0032939641     PISSN: 13891723     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1389-1723(99)80016-4     Document Type: Article
Times cited : (9)

References (7)
  • 1
    • 0014930422 scopus 로고
    • Potent sex attractant of the gypsy moth: Its isolation and synthesis
    • 1. Bierl, B. A., Beroza, M., and Collier, C. W.: Potent sex attractant of the gypsy moth: its isolation and synthesis. Science, 170, 87-89 (1970).
    • (1970) Science , vol.170 , pp. 87-89
    • Bierl, B.A.1    Beroza, M.2    Collier, C.W.3
  • 2
  • 3
    • 0026609017 scopus 로고
    • Large-scale preparation of (+)-disparlure, the gypsy moth pheromone, by a practical chemico-enzymatic procedure
    • 3. Fukusaki, E., Senda, S., Nakazono, Y., Yuasa, H., and Omata, T.: Large-scale preparation of (+)-disparlure, the gypsy moth pheromone, by a practical chemico-enzymatic procedure. J. Ferment. Bioeng., 73, 284-286 (1992).
    • (1992) J. Ferment. Bioeng. , vol.73 , pp. 284-286
    • Fukusaki, E.1    Senda, S.2    Nakazono, Y.3    Yuasa, H.4    Omata, T.5
  • 4
    • 0000962609 scopus 로고
    • Enzymatic resolution of 2,3-epoxyalcohols, intermediates in the synthesis of the gypsy moth sex pheromone
    • 4. Bianchi, D., Cabri, W., Cesti, P., Francalanci, F., and Rama, F.: Enzymatic resolution of 2,3-epoxyalcohols, intermediates in the synthesis of the gypsy moth sex pheromone. Tetrahedron Lett., 29, 2455-2458 (1988).
    • (1988) Tetrahedron Lett. , vol.29 , pp. 2455-2458
    • Bianchi, D.1    Cabri, W.2    Cesti, P.3    Francalanci, F.4    Rama, F.5
  • 5
    • 0026563508 scopus 로고
    • Lipase-catalyzed kinetic resolution of 2,3-epoxy-8-methyl-1-nonanol, the key intermediate n the synthesis of the gypsy moth pheromone
    • 5. Fukusaki, E., Senda, S., Nakazono, Y., Yuasa, H., and Omata, T.: Lipase-catalyzed kinetic resolution of 2,3-epoxy-8-methyl-1-nonanol, the key intermediate n the synthesis of the gypsy moth pheromone. J. Ferment. Bioeng., 73, 280-283 (1992).
    • (1992) J. Ferment. Bioeng. , vol.73 , pp. 280-283
    • Fukusaki, E.1    Senda, S.2    Nakazono, Y.3    Yuasa, H.4    Omata, T.5
  • 6
    • 0019424113 scopus 로고
    • Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycine, erythromycine, leukotriene C-1, and disparlure
    • 6. Rossiter, B. E., Katsuki, T., and Sharpless, K. B.: Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycine, erythromycine, leukotriene C-1, and disparlure. J. Am. Chem. Soc., 103, 464-465 (1981).
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 464-465
    • Rossiter, B.E.1    Katsuki, T.2    Sharpless, K.B.3
  • 7
    • 20644469267 scopus 로고
    • Quantitative analyses of biochemical kinetic resolutions of enantiomer
    • 7. Chen, C.-S., Fujimoto, Y., Girdaukas, G., and Sih, C. J.: Quantitative analyses of biochemical kinetic resolutions of enantiomer. J. Am. Chem. Soc., 104, 7294-7299 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 7294-7299
    • Chen, C.-S.1    Fujimoto, Y.2    Girdaukas, G.3    Sih, C.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.