The Stereochemical Outcome of the DAST Fluorination of 4'-Thiopyrimidine Nucleosides with "Up" Hydroxyl Groups is Controlled by the Oxidation State of the Sulfur Atom

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概要

• 論文の詳細を見る
• 1995-04-05

著者

• JEONG Lak

  Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University

• Marquez Victor

  Laboratory Of Medicinal Chemistry Developmental Therapeutics Program Division Of Cancer Treatment Na

• Jeong Lak

  Laboratory Of Medicinal Chemistry College Of Pharmacy Ewha Womans University

• Jeong L

  Ewha Womans Univ. Seoul. Kor

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• Synthesis of a Rigid Diacylglycerol Analogue Having a Bis-γ-butyrolactone Skeleton Separated by a Cyclopentane Ring
• Preparative Synthesis of the Key Intermediate, (4R, 5R)-3-Benzyloxymethyl-4, 5-isopropylidenedioxycyclopent-2-enone for Carbocyclic Nucleosides
• The Stereochemical Outcome of the DAST Fluorination of 4'-Thiopyrimidine Nucleosides with "Up" Hydroxyl Groups is Controlled by the Oxidation State of the Sulfur Atom

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