Palladium-catalyzed displacement of aryl halide by tin analogue of Reformatsky reagent.
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概要
- 論文の詳細を見る
Reaction of ethyl α-(tributylstannyl)acetate with aryl bromides in the presence of zinc bromide or chloride and a catalytic amount of dichlorobis(tri-<I>o</I>-tolylphosphine)palladium was found to give ethyl arylacetates in good yields except with the aryl bromide having <I>p</I>-acetyl or <I>p</I>-nitro group.
- 公益社団法人 日本化学会の論文
著者
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Kosugi Masanori
Department Of Chemistry Faculty Of Engineering Gunma University
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Kameyama Masayuki
Department of Chemistry, Faculty of Science, Tokyo Metropolitan University
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Migita Toshihiko
Department of Chemistry, Faculty of Engineering, Gunma University
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Negishi Yoshikazu
Department of Chemistry, Faculty of Technology, Gunma University
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