Reaction of azo- and azoxysulfones with transition metal complexes. 4. The reaction of arylazo aryl sulfones with carbon monoxide and nucleophiles catalyzed by the palladium(0) complex.
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概要
- 論文の詳細を見る
The reaction of arylazo aryl sulfone (<B>1</B>) with carbon monoxide in the presence of the palladium(0) catalyst affords substituted benzoic acid in a good yield, together with minor yields of diaryl ketone and biaryl. The reactions of <B>1</B> with carbon monoxide and such nucleophiles as alcohols and amines under similar conditions give esters and amides, respectively.
- 公益社団法人 日本化学会の論文
著者
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Yoshida Masato
Department Of Cardiovascular Surgery Hyogo Brain And Heart Center At Himeji
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Kamigata Nobumasa
Department Of Chemistry Faculty Of Science Tokyo Metropolitan University
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Satoh Akira
Department Of Applied Biochemistry Faculty Of Applied Biological Science Hiroshima University
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Kameyama Masayuki
Department of Chemistry, Faculty of Science, Tokyo Metropolitan University
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