Metalation of Alkylpyridazines. III. Nucleophilic Addition of Lithiated Methylpyridazines and Properties of the Adducts under Basic and Neutral Conditions

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概要

• 論文の詳細を見る

• The reaction of pyridazinylmethyllithiums with ketones in tetrahydrofuran afforded hitherto unaccessible tertiary alcohols in satisfactory yields. The alcohols reverted to methylpyridazines and ketones in a basic medium whereas the alcohols yielded the corresponding dehydrated products (i.e., pyridazinylethylenes) on heating in neutral media.

• 社団法人日本薬学会の論文
• 1979-04-25

著者

• 大沢 昭緒

  School of Pharmaceutical Sciences, Showa University

• 井下田 浩

  School of Pharmaceutical Sciences, Showa University

• 大沢 昭緒

  School Of Pharmaceutical Sciences Showa University

• 井下田 浩

  School Of Pharmaceutical Sciences Showa University

• 上江洲 富夫

  昭和大学薬学部

• 上江洲 富夫

  School of Pharmaceutical Sciences, Showa University

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