Selective hydrogenation of cyclic diolefins to monoolefins catalyzed by a nickel complex.

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概要

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• Cyclic diolefins were hydrogenated selectively to monoolefins with a nickel catalyst prepared from bis(acetylacetonato)nickel(II), triethyldialuminium trichloride, and triphenylphosphine at 40 °C under an atmospheric hydrogen pressure.

• 公益社団法人 日本化学会の論文

著者

• Sakai Mutsuji

  Department Of Polymer Science And Engineering Kyoto Institute Of Technology

• Harada Fumiya

  Department of Polymer Science and Engineering, Kyoto Institute of Technology

• Uchino Norito

  Department of Fiber Chemistry, Kyoto Technical University

• Sakakibara Yasumasa

  Department of Fiber Chemistry, Kyoto Technical University

関連論文

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• The Cyanation of Aromatic Halides Catalyzed by Nickel(0) Complexes Generated In Situ. III. Kinetic and Mechanistic Aspects
• Reduction of Aryl Mesylates Catalyzed by Nickel Complexes
• Studies of the isomerization of unsaturated carboxylic acids. IV. Base-catalyzed rearrangements of .BETA.,.GAMMA.-unsaturated esters to .ALPHA.,.BETA.-isomers.
• Studies on hydrogenation by nickel complexes. 5. The selective hydrogenation of 1,4-cyclohexadienes to cyclohexenes catalyzed by a nickel complex.
• The cyanation of aromatic halides catalyzed by nickel(0) complexes generated in situ. I. General scope and limitations.
• Disproportionation of cyclohexadienes catalyzed by metallic nickel.
• Selective Isomerization of 1,5-Cyclooctadiene to 1,4-Cyclooctadiene Catalyzed by Bis(acetylacetonato)nickel-Triethyldialuminum Trichloride-Phosphorus Ligand.
• Selective hydrogenation of cyclic diolefins to monoolefins catalyzed by a nickel complex.

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