Palladium-catalyzed coupling between organic halides and organotin compounds involving C-N unsaturated bonds at the reaction centers.
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概要
- 論文の詳細を見る
Imidoyl chlorides were good substrates which can react with a variety of organotin compounds to give ketimines in the presence of a catalytic amount of palladium complex. Under similar conditions, <I>C</I>-tributylstannyl imines did not give the products except with 2-(tributylstannyl)benzothiazole, -benzoxazole, and 1-methyl 2-(tributylstannyl)imidazole. And <I>N</I>-tributylstannyl imines could not be utilized.
著者
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Kosugi Masanori
Department Of Chemistry Faculty Of Engineering Gunma University
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Sano Hiroshi
Department Of Biology Faculty Of Science Tohoku University
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Migita Toshihiko
Department of Chemistry, Faculty of Technology, Gunma University
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Koshiba Mamoru
Department of Chemistry, Faculty of Technology, Gunma University
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Atoh Akira
Department of Chemistry, Faculty of Technology, Gunma University
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Migita Toshihiko
Department of Chemistry, Faculty of Engineering, Gunma University
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Sano Hiroshi
Department of Applied Chemistry, Faculty of Engineering, Keio University
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