Magnesium Salt-Induced Opening of α,β-Epoxy Sulfoxides : A Synthesis of α-Chloro Ketones, α-Alkoxy Ketones, and α,β-Unsaturated Ketones from Carbonyl Compounds through α,β-Epoxy Sulfoxides(Organic,Chemical)
スポンサーリンク
概要
- 論文の詳細を見る
Magnesium chloride in alcohols was found to be effective to promote the opening of α,β-epoxy sulfoxides, giving a variety of compounds such as α-chloro ketones, α-alkoxy ketones, or α,β-unsaturated ketones. The products of the reaction were dependent upon the combination of the substituents on the epoxy group of α,β-epoxy sulfoxides, magnesium salt, solvent, and reaction conditions.
- 社団法人日本薬学会の論文
- 1987-11-25
著者
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佐藤 毅
東京理科大学理学部
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佐藤 毅
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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山川 浩司
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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杉本 篤
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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山川 浩司
東京理科大学
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山川 浩司
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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山川 浩司
東京理大
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Satoh T
Department Of Applied Chemistry Faculty Of Engineering Osaka University
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Sato Toshiyuki
Yamagata Research Institute Of Technology
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杉本 篤
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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