A Novel One-pot Synthesis of Cyanohydrin Alkyl Ethers from Aldehydes Catalyzed by Iron(III) Chloride

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概要

• 論文の詳細を見る
• 2004-10-05

著者

• Oriyama Takeshi

  Department Of Chemistry Faculty Of Science Ibaraki University

• Iwanami Katsuyuki

  Department Of Chemistry Faculty Of Science Ibaraki University

• Iwanami Katsuyuki

  Department Of Environmental Sciences Faculty Of Science Ibaraki University

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• Enantioselective Michael Reaction of Malonates and α,β-Unsaturated Aldehydes Using a trans-4-Hydroxyproline Derived Organocatalyst
• One-pot Synthesis of α-Alkoxy Azides from Carbonyl Compounds Catalyzed by Iron(III) Chloride
• A Novel One-pot Synthesis of Cyanohydrin Alkyl Ethers from Aldehydes Catalyzed by Iron(III) Chloride
• Efficient and Enantioselective Kinetic Resolution of Cyclic β-Hydroxy Sulfides by Chiral 1,2-Diamine Catalyzed Asymmetric Acylation
• Michael Addition of Active Methylene Compounds to α,β-Unsaturated Carbonyl Compounds under the Influence of Molecular Sieves in Dimethyl Sulfoxide
• Stepwise Reduction of Acetals to the Corresponding Hydrocarbons. A Mild and Effective Transformation via Carbinyl Bromides.
• The reaction of acetals with silyl enol ethers promoted by the combination of tin(II) chloride and organic halide. Novel and convenient synthesis of .ALPHA.,.BETA.-unsaturated ketones.

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