Amino-Claisen Rearrangement. I

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概要

• 論文の詳細を見る

• Investigation of pyrolytic reactions of N-allylanilinium salts led to the finding of a new type of amino-Claisen rearrangement, aromatic ammonium N-Claisen rearrangement. This reaction enables the introduction of functional group into the ortho position of aniline derivatives. Products are potential precursors for indoline and indole preparations.

• 社団法人日本薬学会の論文
• 1978-07-25

著者

• 片山 肇

  Niigata College Of Pharmacy

• 片山 肇

  新潟薬科大学薬化学教室

• 片山 肇

  Department of Chemistry, University of Alberta

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• 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
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