Novel Oxidative Dimer from Caffeic Acid

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2003 English Publisher:Informa UK LimitedJournal:Bioscience, Biotechnology, and Biochemistry, volume 67, pages 1,185-1,187 (issn: 0916-8451, eissn: 1347-6947,

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Authors: Hiroyuki, Tazaki; Jun, Kawabata; Takashi, Fujita;

doi: 10.1271/bbb.67.1185

pmid: 12834308

Novel Oxidative Dimer from Caffeic Acid

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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.

Related Organizations

Hokkaido Bunkyo University
Japan
Railway Technical Research Institute
Japan
Hokkaido University
Japan
Obihiro University of Agriculture and Veterinary Medicine
Japan

Keywords

Caffeic Acids, Magnetic Resonance Spectroscopy, Iodates, Molecular Conformation, Indicators and Reagents, Oxidation-Reduction

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