Synthesis of Adamantane Derivatives. LXVIII. Cycloaddition Reactions of 2-(1-Adamantyl)-1,3-butadiene and-heterodienes
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概要
- 論文の詳細を見る
2-(1-Adamantyl)-1,3-butadiene (1) was prepared by p-toluenesulfonic acid-catalyzed dehydration of the corresponding allyl alcohol 5. The Diels-Alder reactions of 1 with a variety of dienophiles proceeded smoothly to give adamantane-substituted six-membered carbo-and heterocycles. Similarly, [4+2] cycloaddition reactions of adamantane-bearing heterodienes afforded some adamantyl-oxazines.
- 公益社団法人日本薬学会の論文
- 1984-04-25
著者
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清水 一雄
Institute Of Applied Organic Chemistry Faculty Of Engineering Nagoya University
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佐々木 正
Institute Of Applied Organic Chemistry Faculty Of Engineering Nagoya University
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大野 正富
Institute of Applied Organic Chemistry, Faculty of Engineering, Nagoya University
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大野 正富
Institute Of Applied Organic Chemistry Faculty Of Engineering Nagoya University
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