Total synthesis of (+)-(S)-angustureine and the determination of the absolute configuration of the natural product angustureine

被引：67
|
作者：
Theeraladanon, C [1 ]
Arisawa, M [1 ]
Nakagawa, M [1 ]
Nishida, A [1 ]
机构：
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
来源：
TETRAHEDRON-ASYMMETRY | 2005年 / 16卷 / 04期
关键词：
D O I：
10.1016/j.tetasy.2004.12.022
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
Angustureine, isolated from the bark of Galipea officinalis Hancock, is a novel quinoline alkaloid with a n-pentyl side chain at the 2-position. The total synthesis of (+)-(S)-angustureine and a determination of the absolute configuration of the natural product angustureine were achieved using ring-closing metathesis (RCM) and the Mitsunobu reaction as key steps. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码：827 / 831
页数：5
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