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Volumn 67, Issue 7, 2003, Pages 1559-1567

Synthesis of the four components of the female sex pheromone of the painted apple moth, teia anartoides

Author keywords

Chiral epoxide; Ketone; Painted apple moth; Pheromone; Teia anartoides

Indexed keywords

INSECTA; LEPIDOPTERA; MALUS X DOMESTICA;

EID: 2442499335     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.67.1559     Document Type: Article
Times cited : (14)

References (15)
  • 1
    • 0002773537 scopus 로고
    • The synthesis of insect pheromones
    • ApSimon, J., John Wiley & Sons, New York
    • Mori, K., The synthesis of insect pheromones. In “The Total Synthesis of Natural Products” vol. 4, ed. ApSimon, J., John Wiley & Sons, New York, pp. 60-63 (1981).
    • (1981) The Total Synthesis of Natural Products , vol.4 , pp. 60-63
    • Mori, K.1
  • 2
    • 0000416205 scopus 로고
    • The synthesis of insect pheromones, 1979-1989
    • ApSimon, J., John Wiley & Sons, New York
    • Mori, K., The synthesis of insect pheromones, 1979-1989. In “The Total Synthesis of Natural Products” vol. 9, ed. ApSimon, J., John Wiley & Sons, New York, pp. 165-175 (1992).
    • (1992) The Total Synthesis of Natural Products , vol.9 , pp. 165-175
    • Mori, K.1
  • 3
    • 0017602214 scopus 로고
    • Synthsis of aliphatic insect pheromones from alicyclic starting materials: (Z)-6-Heneicosen-11-one and (Z)-8-dodecenyl acetate
    • Mori, K., Uchida, M., and Matsui, M., Synthsis of aliphatic insect pheromones from alicyclic starting materials: (Z)-6-Heneicosen-11-one and (Z)-8-dodecenyl acetate. Tetrahedron, 33, 385-387 (1977).
    • (1977) Tetrahedron , vol.33 , pp. 385-387
    • Mori, K.1    Uchida, M.2    Matsui, M.3
  • 4
    • 84972934542 scopus 로고
    • A convenient synthesis of the peach fruit moth Carposina niponen-sis Walk. And of the Douglas-fir tussock moth Orgyia pseudotsugata pheromones and analogs
    • Ramiandrasoa, F., and Descoins, C., A convenient synthesis of the peach fruit moth Carposina niponen-sis Walk. and of the Douglas-fir tussock moth Orgyia pseudotsugata pheromones and analogs. Synth. Commun., 20, 1989-1999 (1990).
    • (1990) Synth. Commun. , vol.20 , pp. 1989-1999
    • Ramiandrasoa, F.1    Descoins, C.2
  • 5
    • 0000569063 scopus 로고
    • A d-keto aldehyde synthesis: Application to the preparation of the sex pheromone of the Douglas-fir tussock moth
    • Stowell, J. C., and Polito, M. A., A d-keto aldehyde synthesis: Application to the preparation of the sex pheromone of the Douglas-fir tussock moth. J. Org. Chem., 57, 4560-4562 (1992).
    • (1992) J. Org. Chem. , vol.57 , pp. 4560-4562
    • Stowell, J.C.1    Polito, M.A.2
  • 6
    • 0030971917 scopus 로고    scopus 로고
    • (Z)6,(E)8-Henei-cosadien-11-one: Synergistic sex pheromone component of Douglas-fir tussock moth, Orgyia pseudo-tsugata (McDunnough) (Lepidoptera: Lymantriidae)
    • Gries, G., Slessor, K. N., Gries, R., Khaskin, G., Wimalaratne, P. D. C., Gray, T. G., Grant, G. G., Tracey, A. S., and Hulme, M., (Z)6,(E)8-Henei-cosadien-11-one: Synergistic sex pheromone component of Douglas-fir tussock moth, Orgyia pseudo-tsugata (McDunnough) (Lepidoptera: Lymantriidae). J. Chem. Ecol., 23, 19-34 (1997).
    • (1997) J. Chem. Ecol. , vol.23 , pp. 19-34
    • Gries, G.1    Slessor, K.N.2    Gries, R.3    Khaskin, G.4    Wimalaratne, P.D.C.5    Gray, T.G.6    Grant, G.G.7    Tracey, A.S.8    Hulme, M.9
  • 7
    • 0034717009 scopus 로고    scopus 로고
    • A facile preparation of geometrically pure alkenyl, alkynyl, and aryl conjugated Z-alkenes: Stereospecific synthesis of bombykol
    • Uenishi, J., Kawahama, R., Izaki, Y., and Yonemitsu, O., A facile preparation of geometrically pure alkenyl, alkynyl, and aryl conjugated Z-alkenes: Stereospecific synthesis of bombykol. Tetrahedron, 56, 3493-3500 (2000).
    • (2000) Tetrahedron , vol.56 , pp. 3493-3500
    • Uenishi, J.1    Kawahama, R.2    Izaki, Y.3    Yonemitsu, O.4
  • 8
    • 33644528891 scopus 로고
    • Readily accessible 12-I-51 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
    • 1 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones. J. Org. Chem., 48, 4155-4156 (1983).
    • (1983) J. Org. Chem. , vol.48 , pp. 4155-4156
    • Dess, D.B.1    Martin, J.C.2
  • 9
    • 0037212988 scopus 로고    scopus 로고
    • Synthesis of 6Z,8E-heneicosadien-11-one, a sex phero-mone of the painted apple moth
    • Jury, J. C., Fielder, S., and Vigneswaran, M., Synthesis of 6Z,8E-heneicosadien-11-one, a sex phero-mone of the painted apple moth, Teia anartoides. Tetrahedron Lett., 44, 27-28 (2003).
    • (2003) Teia Anartoides. Tetrahedron Lett. , vol.44 , pp. 27-28
    • Jury, J.C.1    Fielder, S.2    Vigneswaran, M.3
  • 10
    • 0037395147 scopus 로고    scopus 로고
    • Synthesis of all the four stereoisomers of leucomalure [(3Z, 6R *7S*,9R *, 10S*)- and (3Z, 6R *7S*, 9S*, 10R *)-cis-6,7-cis-9,10-diepoxy-3-henicosene], components of the female sex pheromone of the Satin moth, Leucoma salicis
    • Muto, S., and Mori, K., Synthesis of all the four stereoisomers of leucomalure [(3Z, 6R *7S*,9R *, 10S*)- and (3Z, 6R *7S*, 9S*, 10R *)-cis-6,7-cis-9,10-diepoxy-3-henicosene], components of the female sex pheromone of the Satin moth, Leucoma salicis. Eur. J. Org. Chem., 1300-1307 (2003).
    • (2003) Eur. J. Org. Chem. , pp. 1300-1307
    • Muto, S.1    Mori, K.2
  • 11
    • 0000416205 scopus 로고
    • The synthesis of insect pheromones, 1979-1989
    • ApSimon, J., John Wiley & Sons, New York
    • Mori, K., The synthesis of insect pheromones, 1979-1989. In “The Total Synthesis of Natural Products” vol. 9, ed. ApSimon, J., John Wiley & Sons, New York, pp. 94-96 (1992).
    • (1992) The Total Synthesis of Natural Products , vol.9 , pp. 94-96
    • Mori, K.1
  • 12
    • 85004650633 scopus 로고
    • Synthesis of both the enan-tiomers of (Z)-cis-9,10-epoxy-6-heneicosene
    • Ebata, T., and Mori, K., Synthesis of both the enan-tiomers of (Z)-cis-9,10-epoxy-6-heneicosene. Agric. Biol. Chem., 53, 801-804 (1989).
    • (1989) Agric. Biol. Chem. , vol.53 , pp. 801-804
    • Ebata, T.1    Mori, K.2
  • 13
    • 0000587893 scopus 로고
    • Alkylative epoxide rearrangement. A stereospecific approach to chiral epoxide pheromone
    • Bell, T. W., and Ciaccio, J. A., Alkylative epoxide rearrangement. A stereospecific approach to chiral epoxide pheromone. J. Org. Chem., 58, 5153-5162 (1993).
    • (1993) J. Org. Chem. , vol.58 , pp. 5153-5162
    • Bell, T.W.1    Ciaccio, J.A.2
  • 14
    • 52549098710 scopus 로고    scopus 로고
    • A simple synthetic method for chiral 1,2-epoxides and the total synthesis of chiral pheromone epoxide
    • Zhang, Z.-B., Wang, Z.-M., Wang, Y.-X., Liu, H.-Q., Lei, G.-X., and Shi, M., A simple synthetic method for chiral 1,2-epoxides and the total synthesis of chiral pheromone epoxide. J. Chem. Soc. Perkin Trans. 1, 53-57 (2000).
    • (2000) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 53-57
    • Zhang, Z.-B.1    Wang, Z.-M.2    Wang, Y.-X.3    Liu, H.-Q.4    Lei, G.-X.5    Shi, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.