Postulated biogenesis of WS9885B and progress toward an enantioselective synthesis

被引:40
作者
Vanderwal, CD
Vosburg, DA
Weiler, S
Sorensen, EJ
机构
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
D O I
10.1021/ol990723r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
WS9885B promotes the assembly of microtubules in vitro and displays cytotoxicity as potent as paclitaxel against several cancer cell lines. In this Letter, we propose a biogenesis for this architecturally complex bacterial metabolite from a much simpler, polyunsaturated precursor. We also present significant progress toward a convergent, enantioselective synthesis of WS9885B, Our work features a chemoselective palladium-catalyzed cross coupling of two advanced building blocks and an uncommon Claisen-like cyclization.
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页码:645 / 648
页数:4
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