In Situ Protection Methodology in Carbonyl Chemistry

スポンサーリンク

概要

• 論文の詳細を見る

• Recent progress in selective transformation of carbonyl groups using in situ protection methodology is described. These techniques which enable reversing reactivity of functional groups have potential usefulness because they can remove complicated protection–deprotection sequences. In this review, we discuss various in situ protection strategies and their synthetic applications.

著者

• FUJIOKA Hiromichi

  Graduate School of Pharmaceutical Sciences, Osaka University

• Yahata Kenzo

  Graduate School of Pharmaceutical Sciences, Osaka University

関連論文

• Studies on Asymmetric Total Synthesis of Antitumor Antibiotic, Fredericamycin A
• Mild Deprotection of Methylene Acetals in Combination with Trimethylsilyl Triflate–2,2′-Bipyridyl
• P-201 Concise Asymmetric Total Synthesis of Scyphostatin,a Potent Inhibitor of Neutral Sphigomyelinase
• Asymmetric Synthesis by the Intramolecular Haloetherification Reaction of Ene Acetal : Discrimination of Prochiral Dienes in Cyclohexane Systems
• Clean and Direct Synthesis of α,α′-Bithiophenes and Bipyrroles by Metal-Free Oxidative Coupling Using Recyclable Hypervalent Iodine(III) Reagents
• Methodology for in Situ Protection of Aldehydes and Ketones Using Trimethylsilyl Trifluoromethanesulfonate and Phosphines: Selective Alkylation and Reduction of Ketones, Esters, Amides, and Nitriles
• In Situ Protection Methodology in Carbonyl Chemistry

スポンサーリンク