Designer Lewis Acids for Selective Organic Synthesis

スポンサーリンク

概要

• 論文の詳細を見る

• <I>In view of the ever expanding repertoire of Lewis acids available as proton substitutes in current synthetic organic methodology, our goal was to engineer an artificial proton substitute possessing unique topology; effective as an artificial enzyme for chemical reactions, by harnessing the high reactivity of the metal atom towards oxygen and nitrogen. Such a concept was realized by examining the recognition ability of specially designed metal receptors for various oxygen- and nitrogen-containing substrates.</I>

• 社団法人 有機合成化学協会の論文

著者

• ISHIHARA Kazuaki

  School of Engineering, Nagoya University

• YAMAMOTO Hisashi

  School of Engineering, Nagoya University

• Maruoka Keiji

  School of Engineering, Nagoya University

• Yamamoto Hisashi

  School Of Engineering Nagoya University

関連論文

• Tris(pentafluorophenyl)boron as an Efficient, Air Stable, and Water Tolerant Lewis Acid Catalyst
• Regio- and Stereoselective Synthesis of 1,5-Dienes Using Allylic Barium Reagents
• Direct Construction of the Cgrinab Strycture from 1,3-Diene. Regioselective Protonation of Acyclic Polyene
• Synthesis of α-Tocopherol: Scandium(III) Trifluoromethanesulfonate as an Efficient Catalyst in the Reaction of Hydroquinone with Allylic Alcohol
• Aluminum Chloride-Tetraalkylammonium Halide Complex as a Novel Catalyst in Friedel-Crafts Alkylation. Direct Construction of the Chroman Structure from 1,3-Diene
• Metal Ion-Exchanged Montmorillonites as Practical and Useful Solid Catalysis for the Synthesis of α-Tocopherol
• Designer Lewis Acids for Selective Organic Synthesis

スポンサーリンク