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Volumn 8, Issue 8, 1997, Pages 1235-1242

The absolute configuration of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus

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TOXIN;

EID: 0030950489     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00119-5     Document Type: Article
Times cited : (21)

References (15)
  • 2
    • 0343072681 scopus 로고    scopus 로고
    • Optically pure epichlorohydrin is commercially available in both enantiomeric forms from DAISO Corporation, Osaka, Japan. We thank DAISO for the donation of optically pure epichlorohydrin (>98% ee)
    • Optically pure epichlorohydrin is commercially available in both enantiomeric forms from DAISO Corporation, Osaka, Japan. We thank DAISO for the donation of optically pure epichlorohydrin (>98% ee).
  • 4
    • 85007810305 scopus 로고
    • Pertinent reviews utilizing optically active O-benzylglycidol in chiral syntheses, see: Takano, S.; Ogasawara, K. J. Syn. Org. Chem. Jpn. 1989, 47, 813-830: Hanson, R. M. Chem. Rev. 1991, 437-475.
    • (1989) J. Syn. Org. Chem. Jpn. , vol.47 , pp. 813-830
    • Takano, S.1    Ogasawara, K.2
  • 5
    • 0000830825 scopus 로고
    • Pertinent reviews utilizing optically active O-benzylglycidol in chiral syntheses, see: Takano, S.; Ogasawara, K. J. Syn. Org. Chem. Jpn. 1989, 47, 813-830: Hanson, R. M. Chem. Rev. 1991, 437-475.
    • (1991) Chem. Rev. , pp. 437-475
    • Hanson, R.M.1
  • 6
    • 0000321940 scopus 로고
    • Takano, S.; Imamura, Y.; Ogasawara, K. Tetrahedron Lett. 1981, 22, 4479-4482. Takano, S.; Goto, E.; Hirama, M.; Ogasawara, K. Chem. Pharm. Bull. 1982, 30, 2641-2643; Takano, S.; Goto, E.; Ogasawara, K. Tetrahedron Lett. 1982, 23, 5567-5570.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 4479-4482
    • Takano, S.1    Imamura, Y.2    Ogasawara, K.3
  • 7
    • 0020383091 scopus 로고
    • Takano, S.; Imamura, Y.; Ogasawara, K. Tetrahedron Lett. 1981, 22, 4479-4482. Takano, S.; Goto, E.; Hirama, M.; Ogasawara, K. Chem. Pharm. Bull. 1982, 30, 2641-2643; Takano, S.; Goto, E.; Ogasawara, K. Tetrahedron Lett. 1982, 23, 5567-5570.
    • (1982) Chem. Pharm. Bull. , vol.30 , pp. 2641-2643
    • Takano, S.1    Goto, E.2    Hirama, M.3    Ogasawara, K.4
  • 8
    • 0000652590 scopus 로고
    • Takano, S.; Imamura, Y.; Ogasawara, K. Tetrahedron Lett. 1981, 22, 4479-4482. Takano, S.; Goto, E.; Hirama, M.; Ogasawara, K. Chem. Pharm. Bull. 1982, 30, 2641-2643; Takano, S.; Goto, E.; Ogasawara, K. Tetrahedron Lett. 1982, 23, 5567-5570.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 5567-5570
    • Takano, S.1    Goto, E.2    Ogasawara, K.3
  • 9
    • 33847801898 scopus 로고
    • Profitt, J. A.; Watt, D. S.; Corey, E. J. J. Org. Chem. 1975, 40, 127-128: Takano, S.; Yamada, S.; Numata, H.; Ogasawara, K. J. Chem. Soc., Chem. Commun. 1983, 761-763.
    • (1975) J. Org. Chem. , vol.40 , pp. 127-128
    • Profitt, J.A.1    Watt, D.S.2    Corey, E.J.3
  • 14
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    • in press
    • Recently, we have completed an alternative asymmetric synthesis of (+)-sporochnol A by employing the fundamentally different procedure which also supported the present conclusion, see: Kamikubo, T.; Shimizu, M.; Ogasawara, K. Enantiomer, in press.
    • Enantiomer
    • Kamikubo, T.1    Shimizu, M.2    Ogasawara, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.