Asymmetric total synthesis of syringolide 1, a nonproteinaceous elicitor
作者:Jun Ishihara、Tetsuya Sugimoto、Akio Murai
DOI:10.1016/s0040-4020(97)10062-x
日期:1997.11
An asymmetric synthesis of syringolide 1, one of the elicitors produced by Pseudomonas syringae pv. tomato, is described. It was synthesized from 2-(1-oxoethyl)-2-buten-4-olide via 1,4-addition of alkenyl cuprate, asymmetric dihydroxylation, and intramolecular Michael reaction.