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

页码：335 / 336

页数：2

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