Dioxopyrrolines. LX. Cycloaddition Reaction of 4-Benzoyl-5-ethoxycarbonyl-1-phenyl-1H-pyrrole-2,3-dione to Olefins : An Inverse-Electron-Demand Hetero Diels-Alder Reaction
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概要
- 論文の詳細を見る
Thermal cycloaddition of 4-benzoyl-5-ethoxycarbonyl-1-phenyl-1H-Pyrrole-2,3-dione (dioxopyrroline) 1 to electron-rich olefins smoothly proceeded in a highly regio- and stereoselective manner to give pyranopyrrole derivatives in excellent yields. The reaction is a typical inverse-electron-demand hetero Diels-Alder reaction, in which dioxopyrroline behaves as an electron-deficient diene.
- 公益社団法人日本薬学会の論文
- 1996-04-15
著者
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佐野 武弘
昭和薬科大学
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佐野 武弘
Showa Pharmaceutical Univ. Tokyo Jpn
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SANO Takehiro
Showa College of Pharmaceutical Sciences
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HORIGUCHI Yoshie
Showa College of Pharmaceutical Sciences
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Tsuda Yoshisuke
Faculty Of Pharmaceutical Sciences Kanazawa University
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Horiguchi Y
Showa Pharmaceutical University
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