Stable isotope-labeling studies on the oxidative coupling of caffeic acid via o-quinone

Article abstract of DOI:10.1271/bbb.65.2613

The formation of ortho-quinone from ortho-diphenol is a key step in its dimerization. An NMR analysis of the oxidation of 3,4-dihydroxycinnamic acid (caffeic acid) by NaIO₄ revealed the formation of 3-(3′ ,4′-dioxo-1′ ,5′-cyclohexadienyl) prope

Full text of DOI:10.1271/bbb.65.2613

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Bioscience, Biotechnology, and Biochemistry
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Stable Isotope-labeling Studies on the Oxidative
Coupling of Caffeic Acid via o-Quinone
Hiroyuki TAZAKIa, Daisuke TAGUCHIa, Takaomi HAYASHIDAa & Kensuke NABETAa
a Department of Bioresource Science, Obihiro University of Agriculture and Veterinary
Medicine
Published online: 22 May 2014.
To cite this article: Hiroyuki TAZAKI, Daisuke TAGUCHI, Takaomi HAYASHIDA & Kensuke NABETA (2001) Stable Isotope-
labeling Studies on the Oxidative Coupling of Caffeic Acid via o-Quinone, Bioscience, Biotechnology, and Biochemistry,
65:12, 2613-2621, DOI: 10.1271/bbb.65.2613
To link to this article: http://dx.doi.org/10.1271/bbb.65.2613
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