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Volumn 2, Issue 11, 2000, Pages 1633-1636

En Route to a Plant Scale Synthesis of the Promising Antitumor Agent 12,13-Desoxyepothilone B

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; DESOXYEPOTHILONE B; EPOTHILONE B; EPOTHILONE DERIVATIVE; EPOXIDE; LACTONE; THIAZOLE DERIVATIVE;

EID: 0034201169     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0059302     Document Type: Article
Times cited : (55)

References (49)
  • 3
    • 0033550167 scopus 로고    scopus 로고
    • For extensive reviews in this field, see: (a) Nicolaou, K. C.; Roschangar, F.; Vourloumis, D. Angew. Chem., Int. Ed. 1998, 37, 2015. (b) Harris, C. R.; Danishefsky, S. J. J. Org. Chem. 1999, 64, 8434.
    • (1999) J. Org. Chem. , vol.64 , pp. 8434
    • Harris, C.R.1    Danishefsky, S.J.2
  • 5
    • 0032548049 scopus 로고    scopus 로고
    • For some recent total syntheses of epothilone B, see: (a) Mulzer, J.; Mantoulidis, A.; Ohler, E. Tetrahedron Lett. 1998, 39, 8633. (b) White, J. D.; Carter, R. G.; Sundermann, K. F. J. Org. Chem. 1999, 64, 684. (c) May, S. A.; Grieco, P. A. Chem. Commun. 1998, 1597. (d) Sawada, D.; Shibasaki, M. Angew. Chem., Int. Ed. 2000, 39, 209.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 8633
    • Mulzer, J.1    Mantoulidis, A.2    Ohler, E.3
  • 6
    • 0033525108 scopus 로고    scopus 로고
    • For some recent total syntheses of epothilone B, see: (a) Mulzer, J.; Mantoulidis, A.; Ohler, E. Tetrahedron Lett. 1998, 39, 8633. (b) White, J. D.; Carter, R. G.; Sundermann, K. F. J. Org. Chem. 1999, 64, 684. (c) May, S. A.; Grieco, P. A. Chem. Commun. 1998, 1597. (d) Sawada, D.; Shibasaki, M. Angew. Chem., Int. Ed. 2000, 39, 209.
    • (1999) J. Org. Chem. , vol.64 , pp. 684
    • White, J.D.1    Carter, R.G.2    Sundermann, K.F.3
  • 7
    • 0032493824 scopus 로고    scopus 로고
    • For some recent total syntheses of epothilone B, see: (a) Mulzer, J.; Mantoulidis, A.; Ohler, E. Tetrahedron Lett. 1998, 39, 8633. (b) White, J. D.; Carter, R. G.; Sundermann, K. F. J. Org. Chem. 1999, 64, 684. (c) May, S. A.; Grieco, P. A. Chem. Commun. 1998, 1597. (d) Sawada, D.; Shibasaki, M. Angew. Chem., Int. Ed. 2000, 39, 209.
    • (1998) Chem. Commun. , pp. 1597
    • May, S.A.1    Grieco, P.A.2
  • 8
    • 0034598534 scopus 로고    scopus 로고
    • For some recent total syntheses of epothilone B, see: (a) Mulzer, J.; Mantoulidis, A.; Ohler, E. Tetrahedron Lett. 1998, 39, 8633. (b) White, J. D.; Carter, R. G.; Sundermann, K. F. J. Org. Chem. 1999, 64, 684. (c) May, S. A.; Grieco, P. A. Chem. Commun. 1998, 1597. (d) Sawada, D.; Shibasaki, M. Angew. Chem., Int. Ed. 2000, 39, 209.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 209
    • Sawada, D.1    Shibasaki, M.2
  • 19
    • 85037454874 scopus 로고    scopus 로고
    • This work was done in collaboration with Dr. T.-C. Chou, Dr. W. Tong, Dr. O. O'Conner, and Dr. J. Bertino at the Sloan-Kettering Institute for Cancer Research
    • This work was done in collaboration with Dr. T.-C. Chou, Dr. W. Tong, Dr. O. O'Conner, and Dr. J. Bertino at the Sloan-Kettering Institute for Cancer Research.
  • 30
    • 0001594845 scopus 로고
    • Hitherto, glycolates have been prepared by auxiliary chemistry through hydroxylation of the alkanoate rather than through alkylation of the glycolate: Evans, D. A.; Morrissey, M. M.; Dorow, R. L. J. Am. Chem. Soc. 1985, 107, 4346.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 4346
    • Evans, D.A.1    Morrissey, M.M.2    Dorow, R.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.