Rearrangement of 5-isopropenyl-2-norbornene to 5-methyl-3a,4,7,7a-tetrahydro-1H-indene.

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概要

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• The Diels-Alder reaction between cyclopentadiene and isoprene gave predominantly <I>endo</I>- and <I>exo</I>-5-isopropenyl-2-norbornenes and also <I>cis</I>-5-methyltetrahydro-1<I>H</I>-indene produced from the <I>endo</I>-product by Cope rearrangement.

• 公益社団法人 日本化学会の論文

著者

• Ogawa Masaya

  Department Of Neurology Aomori Prefectural Central Hospital

• Iwase Shoji

  Department Of Animal Husbandry Faculty Of Agriculture Tohoku University And Faculty Farm

• Iwase Shoji

  Department of Applied Chemistry, Faculty of Engineering, Kansai University

• Nakata Michihiro

  Department of Applied Chemistry, Faculty of Engineering, Kansai University

• Hamanaka Sawako

  Department of Applied Chemistry, Faculty of Engineering, Kansai University

• Ogawa Masaya

  Department of Applied Chemistry, Faculty of Engineering, Kansai University

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