Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Communications
Novel Oxidative Dimer from Caffeic Acid
Hiroyuki TAZAKI, Jun KAWABATA, Takashi FUJITA
Author information
Keywords: caffeic acid, ortho-quinone, Diels-Alder reaction
JOURNAL FREE ACCESS

2003 Volume 67 Issue 5 Pages 1185-1187

Details
Download PDF (179K)
Download citation RIS

(compatible with EndNote, Reference Manager, ProCite, RefWorks)

BIB TEX

(compatible with BibDesk, LaTeX)

Text
How to download citation
Contact us
Abstract
  The novel Diels-Alder adduct, dicaffeoyl quinone as its hydrate, was formed from the oxidation of 3,4-dihydroxycinnamic acid (caffeic acid) with NaIO4. The structure of this hydrate was determined by spectroscopic methods.
Content from these authors

This article cannot obtain the latest cited-by information.

© 2003 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
Previous article Next article
Favorites & Alerts

Recently viewed articles
Predecessor

Bulletin of the Agricultural Chemical Society of Japan

Agricultural and Biological Chemistry

Share this page
feedback
 Top