The first total synthesis of (±)-terpestacin, HIV syncytium formation inhibitor

被引：24
|
作者：
Tatsuta, K [1 ]
Masuda, N [1 ]
Nishida, H [1 ]
机构：
[1] Waseda Univ, Sch Sci & Engn, Dept Appl Chem, Shinjuku Ku, Tokyo 169, Japan
来源：
TETRAHEDRON LETTERS | 1998年 / 39卷 / 1-2期
关键词：
D O I：
10.1016/S0040-4039(97)10494-4
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
(+/-)-Terpestacin has been synthesized through C-alkylation of beta-keto lactone 9 with chain portion 12. These two compounds were derived from 2-cyclopenten-1-ylactic acid and E,E-farnesol, respectively. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：83 / 86
页数：4
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