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Volumn 4, Issue 16, 2002, Pages 2771-2774

Progress toward the total synthesis of ciguatoxins: A convergent synthesis of the FGHIJKLM ring fragment

Author keywords

[No Author keywords available]

Indexed keywords

CIGUATOXIN; PEPTIDE FRAGMENT;

EID: 0037043549     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026306n     Document Type: Article
Times cited : (59)

References (63)
  • 1
    • 1542502091 scopus 로고
    • For reviews on ciguatoxins and related marine polycyclic ethers, see: (a) Yasumoto, T.; Murata, M. Chem. Rev. 1993, 93, 1897-1909.
    • (1993) Chem. Rev. , vol.93 , pp. 1897-1909
    • Yasumoto, T.1    Murata, M.2
  • 25
    • 0033957108 scopus 로고    scopus 로고
    • For recent synthetic studies from other groups, see: (a) Liu, T.-Z.; Isobe, M. Synlett 2000, 266-268.
    • (2000) Synlett , pp. 266-268
    • Liu, T.-Z.1    Isobe, M.2
  • 53
    • 2042507954 scopus 로고
    • For reviews on Suzuki-Miyaura reaction, see: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483.
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 54
    • 0041503723 scopus 로고    scopus 로고
    • Diedlich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, Chapter 2
    • (b) Suzuki, A. In Metal-Catalyzed Cross-Coupling Reactions; Diedlich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; Chapter 2.
    • (1998) Metal-Catalyzed Cross-Coupling Reactions
    • Suzuki, A.1
  • 56
    • 0035905441 scopus 로고    scopus 로고
    • For a recent comprehensive review on application ot the B-alkyl Suzuki-Miyaura reaction in natural product synthesis, see: Chemler, S. R.; Trauner, D.; Danishefsky, S. J. Angew. Chem., Int. Ed. 2001, 40, 4544-4568.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4544-4568
    • Chemler, S.R.1    Trauner, D.2    Danishefsky, S.J.3
  • 57
    • 0043006462 scopus 로고    scopus 로고
    • note
    • Details of the synthesis of compound 9 are included in Supporting Information.
  • 59
    • 0041503724 scopus 로고    scopus 로고
    • note
    • The corresponding α-diol acetonide was formed in 18% yield, which was potentially useful and could be converted to 4.
  • 60
    • 0042505452 scopus 로고    scopus 로고
    • note
    • 3Al to the oxocarbenium ion from the β-face.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.