The addition reaction of benzynes generated electrochemically from dihalobenzenes with tertiary amines.
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概要
- 論文の詳細を見る
The electroreduction of dihalobenzenes was carried out in the presence of tertiary amines as benzyne acceptors in DMF–TBAP, giving the addition products in yields of more than 10%. For <I>o</I>-dibromobenzene, the yield of the addition product, <I>N</I>-phenylpiperidine, increased to 21% in the presence of <I>N</I>-ethylpiperidine.
- 公益社団法人 日本化学会の論文
著者
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Hori Fumiaki
Department Of Environmental Chemistry And Engineering Faculty Of Engineering Oita Unviersity
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Egashira Naoyoshi
Department Of Applied Chemistry Faculty Of Engineering Oita University
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Takenaga Jun
Department of Environmental Chemistry and Engineering, Faculty of Engineering, Oita University
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