Gollner Andreas, Altmann Karl-Heinz, Gertsch Jürg, Mulzer Johann
University of Vienna, Institute of Organic Chemistry, Währingerstrasse 38, 1090 Vienna, Austria.
Chemistry. 2009 Jun 8;15(24):5979-97. doi: 10.1002/chem.200802605.
We herein describe in full detail the first total synthesis of the antitumor agents neolaulimalide and isolaulimalide as well as a highly efficient route to laulimalide. A Kulinkovich reaction followed by a cyclopropyl-allyl rearrangement is used to install the exo-methylene group. The C(2)-C(16) aldehyde fragment is coupled with the C(17)-C(28) sulfone fragments by a highly (E)-selective Julia-Lythgoe-Kocienski olefination to deliver the key intermediates of all three syntheses. Various conditions for the Yamaguchi macrolactonization are applied to close the individual macrocycles. Finally a carefully elaborated endgame was developed to solve the problem of acyl migration in the case of neolaulimalide. All compounds were tested against several cell lines. The cytotoxicity of neolaulimalide could be confirmed for the first time since its original isolation and it could be shown that it induces tubulin polymerization as efficiently as laulimalide.
我们在此详细描述了抗肿瘤药物新劳利马内酯和异劳利马内酯的首次全合成,以及一条合成劳利马内酯的高效路线。通过库林科维奇反应,随后进行环丙基 - 烯丙基重排来引入亚甲基外双键。C(2)-C(16)醛片段与C(17)-C(28)砜片段通过高度(E)选择性的朱利亚 - 利思戈 - 科钦斯基烯烃化反应偶联,以提供所有三种合成方法的关键中间体。应用了各种条件进行山口大环内酯化反应以闭合各个大环。最后,精心设计了终局策略来解决新劳利马内酯情况下的酰基迁移问题。所有化合物均针对多种细胞系进行了测试。自新劳利马内酯最初分离以来,首次证实了其细胞毒性,并且可以表明它诱导微管蛋白聚合的效率与劳利马内酯相同。