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Volumn 58, Issue 9, 1993, Pages 2468-2477

General Approach to Halogenated Tetrahydrofuran Natural Products from Red Algae of the Genus Laurencia. Total Synthesis of (±)-Kumausallene and (±)-1-epi-Kumausallene

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EID: 0000687526     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00061a021     Document Type: Article
Times cited : (104)

References (53)
  • 8
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    • Scheuer, P. J., Ed.; Academic: New York
    • Moore, R. E. In Marine Natural Products; Scheuer, P. J., Ed.; Academic: New York, 1978; Vol. 1, pp 43–121.
    • (1978) Marine Natural Products , vol.1 , pp. 43-121
    • Moore, R.E.1
  • 9
    • 0000359232 scopus 로고
    • Scheuer, P. J., Ed.; Academic: New York
    • Erickson, F. L. In Marine Natural Products; Scheuer, P. J., Ed.; Academic: New York, 1983; Vol. 5, pp 131–257.
    • (1983) Marine Natural Products , vol.5 , pp. 131-257
    • Erickson, F.L.1
  • 20
    • 0000717321 scopus 로고
    • See, e.g., and references cited therein
    • See, e.g., Krow, G. R. Tetrahedron 1981, 37, 2697 and references cited therein.
    • (1981) Tetrahedron , vol.37 , pp. 2697
    • Krow, G.R.1
  • 41
    • 0019977619 scopus 로고
    • A related sequence was used by Feldman in the synthesis of (±)-panacene, see
    • A related sequence was used by Feldman in the synthesis of (±)-panacene, see: Feldman, K. S.; Mechern, C. C.; Nader, L. J. Am. Chem. Soc. 1982, 104, 4011.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4011
    • Feldman, K.S.1    Mechern, C.C.2    Nader, L.3
  • 48
    • 4644244141 scopus 로고
    • For examples of Mitsunobu inversion in similar systems, see
    • For examples of Mitsunobu inversion in similar systems, see: Jarosz, S.; Glodek, J.; Zamojski, A. Carbohydr. Res. 1987, 163, 289.
    • (1987) Carbohydr. Res. , vol.163 , pp. 289
    • Jarosz, S.1    Glodek, J.2    Zamojski, A.3
  • 52
    • 0002155398 scopus 로고
    • General experimental details were recently described
    • General experimental details were recently described: Fisher, M. J.; Overman, L. E. J. Org. Chem. 1988, 53, 2630.
    • (1988) J. Org. Chem. , vol.53 , pp. 2630
    • Fisher, M.J.1    Overman, L.E.2
  • 53
    • 85022468570 scopus 로고
    • The standard abbreviations employed can be found in, The R*(S*) nomenclature is employed to specify relative configuration of racemic intermediates
    • The standard abbreviations employed can be found in J. Org. Chem. 1992, 57, 14A. The R*(S*) nomenclature is employed to specify relative configuration of racemic intermediates.
    • (1992) J. Org. Chem. , vol.57 , pp. 14A


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.