An Efficient Method for the Synthesis of 3-Mercapto-1-(1,3-thiazolin-2-yl)azetidine Useful for the Pendant Moiety of Oral Carbapenem, L-084

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概要

• 論文の詳細を見る
• Japan Institute of Heterocyclic Chemistryの論文
• 2006-09-01

著者

• Tamai Satoshi

  Medical Research Laboratories Wyeth K.k.

• Kumagai Toshio

  Medical Research Laboratories Wyeth K.k.

• Isoda Takeshi

  Medical Research Laboratories Wyeth K.k.

• Tamai Satoshi

  Medical Research Laboratories

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• Efficient Synthesis of Isothiocyanates Based on the Tandem Staudinger/aza-Wittig Reactions and Mechanistic Consideration of the Tandem Reactions
• A Practical and Facile Synthesis of Azetidine Derivatives for Oral Carbapenem, L-084
• Syntheses and Pharmacokinetic Studies of Prodrug Esters for the Development of Oral Carbapenem, L-084
• An Efficient Method for the Synthesis of 3-Mercapto-1-(1,3-thiazolin-2-yl)azetidine Useful for the Pendant Moiety of Oral Carbapenem, L-084
• New Reaction Mode of the Dieckmann-Type Cyclization under the Lewis Acid-Et_3N Conditions
• Improved Synthesis of an Energetic Material,1,1,3-Trinitroazetidine Exploiting 1-Azabicyclo[1.1.0]butane

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