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Novel oxidative dimer from caffeic acid
Authors:Tazaki Hiroyuki  Kawabata Jun  Fujita Takashi
Affiliation:Department of Bioresource Science, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro 080-8555, Japan. tazaki@obihiro.ac.jp
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.
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