Download PDF
Synlett 1996; 1996(4): 335-336
DOI: 10.1055/s-1996-5430
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Asymmetric Synthesis of Syringolide 1, a Novel Nonproteinaceous Elicitor

Jun Ishihara, Tetsuya Sugimoto, Akio Murai*
  • *Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060, Japan
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

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.

syringolide 1 - elicitor - 1,4-addition - intramolecular Michael reaction

      >