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Oxidative Dimer Produced from a 2,3,4-Trihydroxybenzoic Ester
Title: | Oxidative Dimer Produced from a 2,3,4-Trihydroxybenzoic Ester |
Authors: | KODAMA, Asuka Browse this author | SHIBANO, Hidetoshi Browse this author | KAWABATA, Jun Browse this author →KAKEN DB |
Keywords: | 2,3,4-trihydroxybenzoic acid | phenolic acid | oxidative coupling | DPPH radical | o-chloranil |
Issue Date: | Jul-2007 |
Publisher: | Japan Society for Bioscience, Biotechnology, and Agrochemistry |
Journal Title: | Bioscience, Biotechnology, and Biochemistry |
Volume: | 71 |
Issue: | 7 |
Start Page: | 1731 |
End Page: | 1734 |
Publisher DOI: | 10.1271/bbb.70139 |
Abstract: | The DPPH radical-scavenging abilities of the naturally occurring phenolic acid, 2,3,4-trihydroxybenzoic acid, and its methyl ester were evaluated. Both compounds in acetonitrile scavenged as many as four radicals compared to three or fewer radical consumption in acetone or ethanol. Only the ester showed relatively high ability in methanol. Oxidation with o-chloranil in acetonitrile resulted in methyl 2,3,4-trihydroxybenzoate giving a novel benzocoumarin-type dimer, its chemical structure being confirmed by spectroscopic evidence. The formation of this dimer might partly account for the higher radical-scavenging efficiency of the ester in acetonitrile or methanol. |
Relation: | http://www.jstage.jst.go.jp/ |
Type: | article |
URI: | http://hdl.handle.net/2115/30155 |
Appears in Collections: | 農学院・農学研究院 (Graduate School of Agriculture / Faculty of Agriculture) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 川端 潤
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