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Volumn 3, Issue 15, 2005, Pages 2675-2684

A comparative analysis of the total syntheses of the amphidinolide T natural products

Author keywords

[No Author keywords available]

Indexed keywords

AMPHIDINOLIDE T NATURAL PRODUCTS; C18 POSITION; STRUCTURAL DIVERSITY; TOTAL SYNTHESIS;

EID: 23844495572     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b507315b     Document Type: Review
Times cited : (34)

References (57)
  • 14
    • 33645247933 scopus 로고    scopus 로고
    • Structural revision and synthesis of; (d) amphidinolide A: see ref. 2b
    • Structural revision and synthesis of; (d) amphidinolide A: see ref. 2b;
  • 22
    • 0034629561 scopus 로고    scopus 로고
    • Isolation, structure determination, and biological activity of amphidinolides T1-4: (a) M. Tsuda, T. Endo and J. Kobayashi, J. Org. Chem., 2000, 65, 1349-1352;
    • (2000) J. Org. Chem. , vol.65 , pp. 1349-1352
    • Tsuda, M.1    Endo, T.2    Kobayashi, J.3
  • 24
  • 40
    • 4544323639 scopus 로고    scopus 로고
    • Related nickel-catalyzed coupling reactions have been developed by Montgomery. For a review of these and other nickel-catalyzed reactions, see: J. Montgomery, Angew. Chem., Int. Ed., 2004, 43, 3890-3908.
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 3890-3908
    • Montgomery, J.1
  • 43
    • 0034746687 scopus 로고    scopus 로고
    • and references cited therein
    • T. M. Trnka and R. H. Grubbs, Acc. Chem. Res., 2001, 34, 18-29 and references cited therein.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 18-29
    • Trnka, T.M.1    Grubbs, R.H.2
  • 55
    • 0033616106 scopus 로고    scopus 로고
    • This sequence was performed in analogy to the work of Woerpel, who has synthesized several related cyclic acetals as oxocarbenium ion precursors: C. H. Larsen, B. H. Ridgway, J. T. Shaw and K. A. Woerpel, J. Am. Chem. Soc., 1999, 121, 12208-12209.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 12208-12209
    • Larsen, C.H.1    Ridgway, B.H.2    Shaw, J.T.3    Woerpel, K.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.