메뉴 건너뛰기




Volumn 7, Issue 5, 1999, Pages 665-697

Total synthesis of Epothilone E and related side-chain modified analogues via a stille coupling based strategy

Author keywords

Anticancer agents; Epothilones; Stille coupling; Synthesis

Indexed keywords

ANTINEOPLASTIC AGENT; EPOTHILONE A; EPOTHILONE DERIVATIVE; EPOTHILONE E; LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033135050     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(98)00153-9     Document Type: Article
Times cited : (92)

References (60)
  • 20
    • 0013494582 scopus 로고    scopus 로고
    • For other synthetic approaches to the epothilones, see Ref.
    • For other synthetic approaches to the epothilones, see Ref. .
  • 41
    • 0013560785 scopus 로고    scopus 로고
    • 2O, -78°C)
    • 2O, -78°C).
  • 44
    • 0013494013 scopus 로고    scopus 로고
    • Epothilones 18o and 19o, the products of coupling between stannane 8o and vinyl iodides 7 and 11, respectively, were isolated as C17-methyl ketones and not ethyl enol ethers
    • Epothilones 18o and 19o, the products of coupling between stannane 8o and vinyl iodides 7 and 11, respectively, were isolated as C17-methyl ketones and not ethyl enol ethers.
  • 48
    • 0000434949 scopus 로고
    • Morrison, J. D., Ed.; Orlando: Academic Press
    • (a) Enders, D. In Asymmetric Synthesis; Morrison, J. D., Ed.; Orlando: Academic Press, 1984; 3, p 275.
    • (1984) In Asymmetric Synthesis , vol.3 , pp. 275
    • Enders, D.1
  • 53
    • 0030031287 scopus 로고    scopus 로고
    • We thank Professor D. Enders for a generous gift of SAMP
    • (f) Enders, D.; Backhaus, D.; Runsink, J. Tetrahedron 1996, 52, 1503. We thank Professor D. Enders for a generous gift of SAMP.
    • (1996) Tetrahedron , vol.52 , pp. 1503
    • Enders, D.1    Backhaus, D.2    Runsink, J.3
  • 60
    • 0001974818 scopus 로고
    • For a review of reductions with diimide see
    • For a review of reductions with diimide see: Pasto, D. J.; Taylor, R. T. Org. React. 1991, 40, 91.
    • (1991) Org. React. , vol.40 , pp. 91
    • Pasto, D.J.1    Taylor, R.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.