A NOVEL INVERSE TYPE DIELS-ALDER REACTION OF ETHYL (E)-3-(1,3-BENZOTHIAZOL-2-YL)-3-CYANOPROPENOATE AS A HIGHLY REACTIVE 1-AZA-1,3-BUTADIENE
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概要
- 論文の詳細を見る
Diels-Alder reactions of ethyl (E)-3-(1,3-benzothiazol-2-yl)-3-cyanopropenoate (2) as a 1-aza-1,3-butadiene are described. The diene (2), bearing electron-withdrawing ester group, reacts with electron-rich dienophiles (3a-d) under extremely mild conditions to give corresponding cycloadducts (4a-d) in high yields with high regio- and endo-selectivities. Treatment of 2 with electron-donating allyl alcohols (5a, b) causes tandem transesterification and intramolecular cycloaddition to afford cis-fused polycyclic systems (6a, b) in one step.
- 公益社団法人日本薬学会の論文
- 1995-10-15
著者
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坂本 正徳
Meiji College of Pharmacy
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坂本 正徳
明治薬科大学
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長野 真弓
Meiji College Of Pharmacy
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鈴木 陽子
Meiji College Of Pharmacy
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田村 修
Faculty Of Pharmaceutical Sciences Kanazawa University
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Tamura Osamu
Meiji College Of Pharmacy
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田村 修
Meiji College of Pharmacy
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Sakamoto M
Meiji College Of Pharmacy
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