The acidities of substituted .ALPHA.-phenylsulfinylacetophenones.
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概要
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The acidities of eleven <I>meta</I>- and <I>para</I>-substituted α-phenylsulfinylacetophenones (<B>1</B>) were determined potentiometrically in a 50% ethanol solution. p<I>K</I><SUB>a</SUB> values (10.22–12.01) which can be nicely correlated with Hammett's σ-values were obtained.
- 公益社団法人 日本化学会の論文
著者
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Nokami Junzo
Department Of Applied Chemistry Faculty Of Engineering Okayama University Of Science
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Kinoshita Masayoshi
Department Of Bioapplied Chemistry Faculty Of Engineering Osaka City University
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Kunieda Norio
Department Of Applied Chemistry Faculty Of Engineering Osaka City University
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FUJIWARA YOICHI
Department of Medicinal Chemistry, Kyoto Pharmaceutical University
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Nokami Junzo
Department of Applied Chemistry, Faculty of Engineering, Osaka City University
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Kinoshita Masayoshi
Department of Applied Chemistry, Faculty of Engineering, Osaka City University
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