Updated on 2025/01/21

写真a

 
KATAYAMA Nobuki
 
Organization
Graduate School of Science and Engineering Integrated Science and Engineering
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Research Interests

  • Metal nanopaticles

  • Organometallic chemistry

Education

  • 関西大学大学大学院 博士前期課程

    2022.4 - 2024.3

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  • Kansai University

    2018.4 - 2022.3

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  • 関西大学大学大学院 博士後期課程

    2024.4

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Research History

  • JST SPRING (次世代博士研究員)

    2024.4

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Papers

  • Recyclable and air-stable colloidal manganese nanoparticles catalyzed hydrosilylation of alkenes with tertiary silane

    Nobuki Katayama, Kazuki Tabaru, Tatsuki Nagata, Miku Yamaguchi, Takeyuki Suzuki, Takashi Toyao, Yuan Jing, Zen Maeno, Ken-ichi Shimizu, Takeshi Watanabe, Yasushi Obora

    RSC Advances   2025

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/D4RA08380F

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  • Developments in the synthesis of allylsilanes by transition metal–catalyzed silylation of 1,3-dienes with disilanes

    Nobuki Katayama, Yasushi Obora

    Chemistry Letters   2024.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1093/chemle/upae134

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  • Recent developments in alkene hydrosilylation utilizing manganese catalysts

    Nobuki Katayama, Yasushi Obora

    Tetrahedron Letters   154798 - 154798   2023.10

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Elsevier {BV}  

    DOI: 10.1016/j.tetlet.2023.154798

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  • Dimethylacetamide-stabilized ruthenium nanoparticles for catalysing α-alkylations of amides with alcohols

    Honami Iguchi, Nobuki Katayama, Takeyuki Suzuki, Tetsuaki Fujihara, Yuan Jing, Takashi Toyao, Zen Maeno, Ken-ichi Shimizu, Yasushi Obora

    Chemical Communications   58 ( 84 )   11851 - 11854   2022.9

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry ({RSC})  

    <jats:p>
    <jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>-Dimethylacetamide-stabilized Ru nanoparticles combine the roles of substrate, solvent, and catalyst, and show high activity in the α-alkylation reactions of amides with alcohols.</jats:p>

    DOI: 10.1039/d2cc04133b

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