Asymmetric synthesis of syringolide 1, a novel nonproteinaceous elicitor

被引：0
|
作者：
Ishihara, J [1 ]
Sugimoto, T [1 ]
Murai, A [1 ]
机构：
[1] HOKKAIDO UNIV,GRAD SCH SCI,DIV CHEM,SAPPORO,HOKKAIDO 060,JAPAN
来源：
SYNLETT | 1996年 / 04期
关键词：
syringolide; 1; elicitor; 1,4-addition; intramolecular Michael reaction;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An asymmetric synthesis of syringolide 1, a novel nonproteinaceous elicitor, is described. It was synthesized from 2-(1-oxoethyl)-2-buten-4-olide via 1,4-addition of alkenyl cuprate and intramolecular Michael reaction.
引用
收藏
页码：335 / 336
页数：2
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