Antioxidant Activities of Dihydric Phenol Derivatives for the Autoxidation of Tetralin.

…, S Terauchi, S Tomiyama, T Nishiyama

Index: Yamamura; Nishiwaki; Tanigaki; Terauchi; Tomiyama; Nishiyama Bulletin of the Chemical Society of Japan, 1995 , vol. 68, # 10 p. 2955 - 2960

Full Text: HTML

Citation Number: 9

Abstract

The antioxidant activities of dihydric phenols, such as catechol, resorcinol, and hydroquinone, and their twenty-three alkyl and benzyl substituted derivatives were evaluated by means of an oxygen-absorption method at 60° C for determining the oxidation of tetralin. Catechols exhibited a much higher stoichiometric factor (2.0—2.3) compared with those of other compounds. The stoichiometric factors of hydroquinones (0.6—1.1) are ...

Related Articles:

A convenient synthesis of 2-alkylated 1, 4-benzenediols

[Ozaki, Yutaka; Hosoya, Ayako; Okamura, Kyouko; Kim, Sang-Won Synlett, 1997 , vol. 1997, # 4 p. 365 - 366]

Acid-induced rearrangement reactions of reduced benzoquinone cyclopentadiene cycloadducts

[Al-Hamdany, Raad; Bruce, J. Malcolm; Heatley, Frank; Khalafy, Jabbar Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1985 , p. 1395 - 1400]

Evidence for single electron transfer (SET) pathway in the reaction of primary alkylcadmium reagents with p-benzoquinone

[Shahidzadeh, Mansour; Ghandi, Mehdi Journal of Organometallic Chemistry, 2001 , vol. 625, # 1 p. 108 - 111]

More Articles...