Synthetic studies toward the microtubule-stabilizing agent laulimalide:: synthesis of the C1-C14 fragment

被引:37
作者
Nadolski, GT [1 ]
Davidson, BS [1 ]
机构
[1] Utah State Univ, Dept Chem & Biochem, Logan, UT 84322 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0040-4039(00)02116-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The C-1-C-14 fragment of the paclitaxel-like antimicrotubule agent laulimalide has been synthesized in 15 steps from L-(-)-citronellal. The C-9 chiral center was established using an asymmetric allylation, the dihydropyran ring was prepared through ring-closing metathesis. and the no-methylene was incorporated using Eschenmoser's salt. (C) 2001 Published by Elsevier Science Ltd.
引用
收藏
页码:797 / 800
页数:4
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