Amino-Claisen Rearrangement. V. Rearrangement of Substituted Tetrahydroquinolines Involving Competitive Cope Rearrangement in a Reaction Intermediate

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概要

• 論文の詳細を見る

• A competitive Cope rearrangement was observed during Claisen rearrangement of substituted tetrahydroquinolines. It was found that the introduction of an ethyl group onto the methylene of the migrating allylic moiety greatly accelerated the Cope rearrangement. At the same time, replacement of the 1-ethyl-2-propenyl group on the aromatic ring by a 1-propenyl (allyl) group was observed.

• 社団法人日本薬学会の論文
• 1984-06-25

著者

• 金子 喜三好

  Niigata College Of Pharmacy

• 片山 肇

  Niigata College Of Pharmacy

• 片山 肇

  新潟薬科大学薬化学教室

• 樋口 由昭

  Niigata College of Pharmacy

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