A NOVEL CARBON-CARBON BOND FORMATION AT THE C4 POSITION OF β-LACTAMS. FLUORIDE ION INDUCED DESILYLATIVE α-HYDROXYALKYLATION OF 3-ALKYLIDENE-4-TRIMETHYLAZETIDIN-2-ONES WITH ALDEHYDES

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概要

• 論文の詳細を見る

• the reaction of 3-alkylidene-4-trimethylsilylazetidin-2-ones with aldehydes in the presence of fluoride ion gave 3-alkylidene-4-(α-hydroxy)-alkylazetidin-2-ones in good to moderate yields.

• 公益社団法人日本薬学会の論文
• 1996-02-15

著者

• Suda K

  Meiji Coll. Pharmacy Tokyo

• HOTODA Katsumi

  Shiratori Pharmaceutical Co., Ltd.,

• AOYAGI Mitsuaki

  Meiji College of Pharmacy

• TAKANAMI Toshikatsu

  Meiji College of Pharmacy

• SUDA Kohji

  Meiji College of Pharmacy

• Hotoda K

  Shiratori Pharmaceutical Co. Ltd.

• Aoyagi M

  Meiji College Of Pharmacy

• Takanami T

  Meiji Coll. Pharmacy Tokyo

関連論文

• A NOVEL CARBON-CARBON BOND FORMATION AT THE C4 POSITION OF β-LACTAMS. FLUORIDE ION INDUCED DESILYLATIVE α-HYDROXYALKYLATION OF 3-ALKYLIDENE-4-TRIMETHYLAZETIDIN-2-ONES WITH ALDEHYDES
• A Novel Electrochemical Oxidation Reactions Utilizing Cyclodextrins. Anodic Oxidation of Indole-Cyclodextrin-Alcohol System

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