Stable Sulfur Ylides. III. Reaction of Stable Sulfonium Allylides and Oxosulfonium Allylides with Alkoxides
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概要
- 論文の詳細を見る
Treatment of dimethyloxosulfonium 1-benzoyl-3,3-diacylallylides (Ia-b) with sodium ethoxide in ethanol or sodium methoxide in methanol gave several thiabenzene 1-oxide derivatives (IIa-b, IIIa-d). Similar treatment of dimethyloxosulfonium 1-benzoyl-3-acetylallylide (Ic) afforded 1,5-dimethyl-2-benzoylthiabenzene 1-oxide (IIIe) in a good yield. On the other hand, treatment of dimethyl-and tetramethylene-sulfonium 1-benzoyl-3,3-diacylallylides (Va-c) with sodium ethoxide in ethanol gave biphenyl derivatives (VIa-c).
- 公益社団法人日本薬学会の論文
- 1975-02-25
著者
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木下 敏夫
Faculty of Pharmaceutical Sciences, Nagasaki University
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古川 淳
Faculty of Pharmaceutical Sciences, Nagasaki University
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渡辺 三明
Faculty of Pharmaceutical Sciences
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木下 敏夫
School of Pharmaceutical Sciences, Nagasaki University
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渡辺 三明
Center For Instrumental Analysis Nagasaki University
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木下 敏夫
School Of Pharmaceutical Sciences Nagasaki University
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