Convenient Synthesis of 4-Alkyl, Alkenyl, and Alkynyl Substituted N-(Phenylsulfonyl)indoles
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概要
- 論文の詳細を見る
The indolone 1 reacted with organomagnesium or lithium reagents to give the carbinols 6 and 10,which, upon treatment under appropriate acidic conditions or neutral thermal conditions, gave the 1-phenylsulfonylindoles 8 and 11 bearing various kinds of alkyl, alkenyl, and alkynyl substituents at the 4-position. The indolone 1 was also converted to the 4-cyanoindole 14 via the cyanohydrin O-trimethylsilyl ether 13.
- 社団法人日本薬学会の論文
- 1994-10-15
著者
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池田 正澄
Kyoto Pharmaceutical University
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池田 正澄
京都薬科大学
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石橋 弘行
Kyoto Pharmaceutical University
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石橋 弘行
金沢大学薬学部
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石橋 弘行
京都薬科大学
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赤松 進
Kyoto Pharmaceutical University
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入山 浩子
Kyoto Pharmaceutical University
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