Trifluoromethanesulfonic Anhydride-Promoted α-Bromination of Ketones with Grignard Reagent or Magnesium Bromide
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概要
- 論文の詳細を見る
The direct α-bromination of various ketones using trifluoromethanesulfonic anhydride and Grignard reagent or magnesium bromide in ether gave the corresponding α-bromo ketones in moderate to good yields under mild reaction conditions.
- 公益社団法人日本薬学会の論文
- 2000-12-01
著者
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Kimura S
Department Of Applied Chemistry Faculty Of Engineering & High Technology Research Center Kansai
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Kimura Saori
Department Of Anesthesia Muroran City General Hospital
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ONO Yasuhiro
Department of Applied Physics, Graduate School of Engineering, Tohoku University
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NISHIYAMA Tomihiro
Department of Applied Chemistry, Faculty of Engineering, Kansai University
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KUROKAWA Sachiko
Department of Applied Chemistry, Faculty of Engineering & High Technology Research Center, Kansai Un
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Kurokawa Sachiko
Department Of Applied Chemistry Faculty Of Engineering & High Technology Research Center Kansai
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Nishiyama T
Department Of Applied Chemistry Faculty Of Engineering And High Technology Research Center Kansai Un
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Nishiyama Tomihiro
Department Of Applied Chemistry Faculty Of Engineering & High Technology Research Center Kansai
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Nishiyama Tomihiro
Department Of Applied Chemistry
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Ono Yasuhiro
Department Of Applied Chemistry Faculty Of Engineering & High Technology Research Center Kansai
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