Intramolecular Cycloaddition of 2-Allylphenylhydrazones

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概要

• 論文の詳細を見る

• Acid-catalyzed intramolecular cycloaddition of 2-allylphenylhydrazones is an effective method for the preparation of 2,3,3a, 4-tetrahydro-1H-pyrazolo[1,5-α]indole derivatives.

• 社団法人日本薬学会の論文
• 1990-05-25

著者

• 片山 肇

  Niigata College Of Pharmacy

• 片山 肇

  新潟薬科大学薬化学教室

• 高津 徳行

  Niigata College of Pharmacy

• 北野 晴子

  Niigata College of Pharmacy

• 嶋谷 ゆかり

  Niigata College of Pharmacy

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• βアドレナリン受容体遮断薬の分子薬理
• Amino-Claisen Rearrangement. V. Rearrangement of Substituted Tetrahydroquinolines Involving Competitive Cope Rearrangement in a Reaction Intermediate
• Amino-Claisen Rearrangement. IV. Quaternary Amino-Claisen Rearrangement of N-Allyljulolidinium Derivatives
• Vilsmeier-Haack-Arnold and Bromination Reactions of 4H-Pyrazolo[1,5-a]indole Derivatives
• Preparation and Reaction of 3-Oxo-3H-pyrazolo[1,5-a]indole Derivatives
• Preparation and Reactions of 3H-Pyrazolo[1,5-a]indole Derivatives
• Fischer Indolization of N^α-Alkyl-2-allylphenylhydrazones
• Molecular Structure of a Novel Indole Derivative, (2SR, 3aSR)-2-Phenyl-2,3,3a, 4-tetrahydro-1H-pyrazolo[1,5-a]indole
• 1H-PYRAZOLO[1,5-α]INDOLES : ISOELECTRONIC ANALOGUES OF AZULENE (PSEUDOAZULENE)
• Preparation of 4H-Pyrazolo[1,5-α]indole
• Intramolecular Cycloaddition of 2-Allylphenylhydrazones
• Amino-Claisen Rearrangement. III. The Effects of Alkyl Substituents on the Allyl Group upon the Rearrangement
• Amino-Claisen Rearrangement. II. Quaternary Amino-Claisen Rearrangement of Anilinium Compounds with ortho Substituents
• Amino-Claisen Rearrangement. I
• A Convenient Preparation of N-Acyl-1,2-dihydroquinoline
• イモノキ(タカノツメ)Evodiopanax innovans NAKAIの成分研究(第1報) : 葉からMaltolとRhoifolinの単離

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