A highly stereoselective synthesis of epothilone B

被引:78
作者
White, JD [1 ]
Carter, RG [1 ]
Sundermann, KF [1 ]
机构
[1] Oregon State Univ, Dept Chem, Corvallis, OR 97331 USA
关键词
D O I
10.1021/jo982108r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:684 / 685
页数:2
相关论文
共 28 条
  • [21] Nicolaou KC, 1998, ANGEW CHEM INT EDIT, V37, P2015, DOI 10.1002/(SICI)1521-3773(19980817)37:15<2014::AID-ANIE2014>3.0.CO
  • [22] 2-2
  • [23] Total synthesis of 26-hydroxy-epothilone B and related analogs via a macrolactonization based strategy
    Nicolaou, KC
    Finlay, MRV
    Ninkovic, S
    Sarabia, F
    [J]. TETRAHEDRON, 1998, 54 (25) : 7127 - 7166
  • [24] Total syntheses of epothilones A and B via a macrolactonization-based strategy
    Nicolaou, KC
    Ninkovic, S
    Sarabia, F
    Vourloumis, D
    He, Y
    Vallberg, H
    Finlay, MRV
    Yang, Z
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (34) : 7974 - 7991
  • [25] Studies towards the total synthesis of epothilones: Asymmetric synthesis of the key fragments
    Schinzer, D
    Limberg, A
    Bohm, OM
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 1996, 2 (11) : 1477 - 1482
  • [26] Schinzer D, 1998, SYNLETT, P861
  • [27] Towards the synthesis of epothilone A: Enantioselective preparation of the thiazole sidechain and macrocyclic ring closure
    Taylor, RE
    Haley, JD
    [J]. TETRAHEDRON LETTERS, 1997, 38 (12) : 2061 - 2064
  • [28] WHITE JD, 1993, SYNLETT, P535