Lewis Acid-Promoted Cycloaddition Reaction of Cyclopropanes with Allylsilanes

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概要

• 論文の詳細を見る

• The treatment of cyclopropanes having donor and acceptor substituents at the vicinal positions on the cyclopropane ring with a Lewis acid readily generates a 1, 3-zwitterion, which reacted with allylsilanes to produce cycloadducts and allylic products. It was found that the yield of the cycloadduct depends on the steric demand of the alkyl substituents on the silicon atom.

• 公益社団法人日本薬学会の論文
• 2001-05-01

著者

• Yokoe Ichiro

  Faculty of Pharmaceutical Science, Josai University

• SUGITA Yoshiaki

  Faculty of Pharmaceutical Sciences, Josai University

• Yokoe I

  Faculty Of Pharmaceutical Sciences Josai University

• Sugita Yoshiaki

  Faculty Of Pharmaceutical Sciences Josai University

• Sugita Y

  Faculty Of Pharmaceutical Sciences Josai University

• Hosoya H

  Faculty Of Pharmaceutical Sciences Josai University

• YAMADOI Shiori

  Faculty of Pharmaceutical Sciences, Josai University

• HOSOYA Hiroki

  Faculty of Pharmaceutical Sciences, Josai University

• Yamadoi Shiori

  Faculty Of Pharmaceutical Sciences Josai University

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