Novel Rearrangements of α-N-Alkylamido-substituted Sulfides and Sulfones

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概要

• 論文の詳細を見る

• The present paper describes novel rearrangements of α-N-alkylamido-substituted sulfides and sulfones promoted by strong bases such as NaH, lithium diisopropylamide and butyllithium, where the alkyl group linked to the sulfur migrates to the amide carbonyl carbon to give the corresponding ketones. The reactions are established as intramolecular rearrangements, and the mechanism is discussed.

• 社団法人日本薬学会の論文
• 1981-09-25

著者

• 関屋 実

  School Of Pharmaceutical Sciences University Of Shizuoka

• 鈴木 邦夫

  School Of Pharmaceutical Sciences University Of Shizuoka

• 石河 芳治

  Shizuoka College of Pharmacy

• 寺尾 良保

  Shizuoka College of Pharmacy

• 鈴木 邦夫

  Shizuoka College of Pharmacy

• 関屋 実

  Shizuoka College of Pharmacy

• 紅林 泰生

  Shizuoka College of Pharmacy

• 寺尾 良保

  School Of Pharmaceutical Sciences University Of Shizuoka

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