Trifluoroacetic Acid-Catalyzed 1,3-Cycloaddition of the Simplest Iminium Ylide Leading to 3-or 3,4-Substituted Pyrrolidines and 2,5-Dihydropyrroles
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概要
- 論文の詳細を見る
The 1,3-dipolar cycloaddition of an intermediary iminium ylide formed from N-benzyl-N-(methoxymethyl) trimethylsilylmethylamine to conjugated olefinic and acetylenic dipolarophiles in the presence of a catalytic amount of trifluoroacetic acid has been found to give 3-or 3,4-substituted pyrrolidines and 2,5-dihydropyrroles.
- 公益社団法人日本薬学会の論文
- 1985-07-25
著者
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今井 信行
Shizuoka College Of Pharmacy
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寺尾 良保
Shizuoka College of Pharmacy
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寺尾 良保
School Of Pharmaceutical Sciences University Of Shizuoka
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阿知波 一雄
Shizuoka College of Pharmacy
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小滝 浩美
Shizuoka College of Pharmacy
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