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  1. 1100 学部・機構・専門職大学院
  2. 理工系学部
  3. 関西大学工学研究報告 = Technology reports of the Kansai University
  4. 第47号

Antioxidant Activity and Oxidation Products of 1,2,3,4- Tetrahydroquinoxalines in Peroxyl Radical Scavenging Reactions, Part I

http://hdl.handle.net/10112/11825
http://hdl.handle.net/10112/11825
3089a205-50ef-4fea-b5d2-aa275f9def80
名前 / ファイル ライセンス アクション
KU-1100-20050321-05.pdf KU-1100-20050321-05.pdf (790.0 kB)
Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2018-01-26
タイトル
タイトル Antioxidant Activity and Oxidation Products of 1,2,3,4- Tetrahydroquinoxalines in Peroxyl Radical Scavenging Reactions, Part I
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
著者 Sakata, Toshifumi

× Sakata, Toshifumi

WEKO 28123

Sakata, Toshifumi

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Tanaka, Daisuke

× Tanaka, Daisuke

WEKO 28124

Tanaka, Daisuke

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Takahashi, Masamitsu

× Takahashi, Masamitsu

WEKO 28125

Takahashi, Masamitsu

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Sakaguchi, Tomoki

× Sakaguchi, Tomoki

WEKO 28126

Sakaguchi, Tomoki

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Oka, Ryohei

× Oka, Ryohei

WEKO 28127

Oka, Ryohei

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Nishiyama, Tomohiro

× Nishiyama, Tomohiro

WEKO 28128

Nishiyama, Tomohiro

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概要
内容記述タイプ Other
内容記述 This paper studies the antioxidant activity of 1,2,3,4-tetrahydroquinolines, 3,4-dihydro-2H-benzo[1,4]thiazines and 1,2,3,4-tetrahydroquinoxalines in the inhibition of the peroxidation of tetralin induced by an azo initiator. Neither 1,2,3,4- tetrahydroquinoline nor 3,4-dihydro-2H-benzo[1,4]thiazine alone acted as an antioxidant, but when they have an electron-donating group at the para position to the NH group, they act as potent antioxidants. On the other hand, 1,2,3,4- tetrahydroquinoxaline on its own showed good antioxidant activity. However, 1,2,3,4-tetrahydroquinoxalines with methyl and methoxy groups in the phenyl ring have reactivities similar to or less than that of unsubstituted 1,2,3,4-tetrahydroquinoxaline. The induction periods of 1,2,3,4-tetrahydroquinoxalines with an alkyl group or phenyl group at the 2-position were all longer than the value for the unsubstituted 1,2,3,4-tetrahydroquinoxaline, except for a compound with a t-butyl group. The oxidation of 1,2,3,4-tetrahydroquinoxalines by peroxyl radicals generated from an azo initiator in tetralin or benzene yields quinoxalines and a dimer product of quinoxalines, 6-(1,2,3,4-tetrahydroquinoxalin-1-yl)-quinoxaline.
書誌情報 関西大学工学研究報告 = Technology reports of the Kansai University

巻 47, p. 39-48, 発行日 2005-03-21
ISSN
収録物識別子タイプ ISSN
収録物識別子 04532198
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AN00046916
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
出版者
出版者 関西大学工学部
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