Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Regular Papers
Synthesis of (±)-Sundiversifolide Based on Lewis Acid-Mediated Claisen Rearrangement
Takashi HASHIMOTOTakuya TASHIROMitsuru SASAKIHirosato TAKIKAWA
Author information
JOURNAL FREE ACCESS

2007 Volume 71 Issue 8 Pages 2046-2051

Details
Abstract

A new and concise synthesis of (±)-sundiversifolide (1), an allelopathic bisnor-sesquiterpene lactone isolated from germinating sunflower (Helianthus annuus L.) seeds, was achieved by employing Lewis acid-mediated Claisen rearrangement as the key step.

Content from these authors

This article cannot obtain the latest cited-by information.

© 2007 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
Previous article Next article
feedback
Top