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Volumn 72, Issue 2, 2007, Pages 640-642

Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGENATION; SYNTHESIS (CHEMICAL);

EID: 33846210688     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0620415     Document Type: Article
Times cited : (35)

References (39)
  • 10
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    • For elegant examples involving catalytic reactions, see: a
    • For elegant examples involving catalytic reactions, see: (a) Burke, S. D.; Müller, N.; Beaudry, C. M. Org. Lett. 1999, 1, 1827-1829.
    • (1999) Org. Lett , vol.1 , pp. 1827-1829
    • Burke, S.D.1    Müller, N.2    Beaudry, C.M.3
  • 18
    • 33947486579 scopus 로고    scopus 로고
    • Anhydrous glutaraldehyde 1a (n = 1) was prepared from its 50% aqueous solution: (a) House, H. O.; Cronin, T. H. J. Org. Chem. 1965, 30, 1061-1070.
    • Anhydrous glutaraldehyde 1a (n = 1) was prepared from its 50% aqueous solution: (a) House, H. O.; Cronin, T. H. J. Org. Chem. 1965, 30, 1061-1070.
  • 19
    • 23044484321 scopus 로고    scopus 로고
    • 1b and 1d (n = 2, 4) were obtained by periodate cleavage of the corresponding cyclo-1,2-diols: Lopez, S.; Fernandez-Trillo, F.; Midon, P.; Castedo, L.; Saa, C. J. Org. Chem. 2005, 70, 6346-6352.
    • 1b and 1d (n = 2, 4) were obtained by periodate cleavage of the corresponding cyclo-1,2-diols: Lopez, S.; Fernandez-Trillo, F.; Midon, P.; Castedo, L.; Saa, C. J. Org. Chem. 2005, 70, 6346-6352.
  • 20
    • 0036382537 scopus 로고    scopus 로고
    • 1c and 1e were obtained from IBX oxidation of the corresponding diols: (b) Lafont, D.; Chevalier, Y.; Grumel, V.; Cassel, S.; Rollin, P. Synth. Commun. 2002, 32, 2919-2930.
    • 1c and 1e were obtained from IBX oxidation of the corresponding diols: (b) Lafont, D.; Chevalier, Y.; Grumel, V.; Cassel, S.; Rollin, P. Synth. Commun. 2002, 32, 2919-2930.
  • 21
    • 85004434318 scopus 로고    scopus 로고
    • We have stored this material in the freezer over several weeks without any detectable decomposition, a Iriye, R, Toya, T, Makino, J, Aruga, R, Doi, Y, Handa, S, Tanaka, H. Agric. Biol. Chem. 1988, 52, 989-996
    • We have stored this material in the freezer over several weeks without any detectable decomposition, (a) Iriye, R.; Toya, T.; Makino, J.; Aruga, R.; Doi, Y.; Handa, S.; Tanaka, H. Agric. Biol. Chem. 1988, 52, 989-996.
  • 25
    • 85004637496 scopus 로고    scopus 로고
    • 5a: (a) Ando, T.; Koike, M.; Uchiyama, M.; Kuroko, H. Agric. Biol. Chem. 1987, 51, 2691-2694.
    • 5a: (a) Ando, T.; Koike, M.; Uchiyama, M.; Kuroko, H. Agric. Biol. Chem. 1987, 51, 2691-2694.
  • 26
    • 84998259475 scopus 로고    scopus 로고
    • 5b: (b) Ando, T.; Katagiri, Y.; Uchiyama, M. Agric. Biol. Chem. 1985, 49, 413-422.
    • 5b: (b) Ando, T.; Katagiri, Y.; Uchiyama, M. Agric. Biol. Chem. 1985, 49, 413-422.
  • 27
    • 0036307526 scopus 로고    scopus 로고
    • 5c: ref 4. 5d: (c) Santangelo, E. M.; Coracini, M.; Witzgall, P.; Correa, A. G.; Unelius, C. R. J. Nat. Prod. 2002, 65, 909-915.
    • 5c: ref 4. 5d: (c) Santangelo, E. M.; Coracini, M.; Witzgall, P.; Correa, A. G.; Unelius, C. R. J. Nat. Prod. 2002, 65, 909-915.
  • 29
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    • 5e: (e) Cabezas, J. A.; Oehlschlager, A. C. Synthesis 1999, 107-111.
    • 5e: (e) Cabezas, J. A.; Oehlschlager, A. C. Synthesis 1999, 107-111.
  • 30
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    • 5f: (f) Michelot, D. Synthesis 1983, 130-134.
    • 5f: (f) Michelot, D. Synthesis 1983, 130-134.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.