FACILE OXY-VINYL[1,3]SHIFT PROMOTED BY TETRABUTYLAMMONIUM FLUORIDE : A HYDROINDOLE SYNTHESIS
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概要
- 論文の詳細を見る
The oxy-vinyl alkoxides generated from trimethylsilyloxy-vinyl (or methoxyvinyl)-cyclobutanes by tetra-n-butylammonium fluoride undergo a facile[1,3]shift to produce a two-carbon unit ring expansion compound under extremely mild conditions. Thus, 7-trimethylsilyloxy-7-vinyl (or methoxyvinyl)-2-azabicyclo[3.2.0]heptane-3,4-diones readily gave hydroindole derivatives in good yields.
- 公益社団法人日本薬学会の論文
- 1983-08-25
著者
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津田 喜典
Faculty of Pharmaceutical Sciences, Kanazawa University
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津田 喜典
Faculty Of Pharmaceutical Sciences Kanazawa University
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佐野 武弘
Showa College of Pharmaceutical Sciences.
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津田 喜典
金沢大薬
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戸田 潤
Showa College of Pharmaceutical Sciences
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佐野 武弘
Showa College Of Pharmaceutical Sciences
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