服部 倫弘 (Tomohiro Hattori)

お知らせ

    研究テーマ

    金属触媒的新規基質支配反応の開発

    略歴

    2013年3月岐阜薬科大学薬学部薬学科 卒業
    2017年3月岐阜薬科大学大学院薬学研究科博士課程 修了 博士(薬学)
    服部倫弘

    職歴

    2015年4月日本学術振興会特別研究員(DC2)
    2017年4月中部大学分子性触媒研究センター 特任助教(山本尚教授)
    2020年4月中部大学分子性触媒研究センター 特任講師(山本尚教授)

    Objective

    Metal Catalyzed Substrate-Controlled Reactions

    Degree

    2013B.Pharm Sc. Gifu Pharmaceutical University, Gifu, Japan
    2017Ph.D. Gifu Pharmaceutical University, Gifu, Japan (Pharmacy)

    Experience

    2015-2017Research Fellow of the Japan Society for the Promotion of Science (DC2)
    2017-2020Research Assistant professsor
    Chubu University (Japan) PI: Prof. Hisashi Yamamoto
    2020-Senior assistant professsor
    Chubu University (Japan) PI: Prof. Hisashi Yamamoto

    List of Publications and Awards

    21. Thieme Chemistry Journals Award 2023.

    20. Silicon-based hydrophobic tags applied in liquid-phase peptide synthesis: protected DRGN-1 and poly alanine chain synthesis. A. Wu, I. Ramakrishna, T. Hattori, H. Yamamoto, Org. Biomol. Chem., 2022, 20, 8685-8692.

    19. Synthesis of Silacyclic Dipeptides: Peptide Elongation at Both N- and C-Termini of Dipeptide. T. Hattori, H. Yamamoto, J. Am. Chem. Soc2022144, 1758-1765.

    18.Amide bond formation: beyond the dilemma between activation and racemisation, W. Muramatsu, T. Hattori, H. Yamamot, Chem. Commun.. 202157, 6346-6359.

    17. Regio- and Stereoselective (SN2) N-, O-, C- and S-Alkylation using Trialkyl Phosphates, A. Banerjee, T. Hattori, H. Yamamoto,Synthesis2021, A-R.

    16. 基質支配的アミド結合形成反応:ペプチド合成の新機軸, T. Hattori, W. Muramatsu,  H. Yamamoto, 有機合成化学協会誌, 202179, 382-390

    15. Game Change from Reagent- to Substrate-Controlled Peptides Synthesis, W. Muramatsu, T. Hattori, H. Yamamoto, Bull. Chem. Soc. J., 202093, 759-767.

    14. Substrate-Directed Lewis-Acid Catalysis for Peptide Synthesis, W. Muramatsu, T. Hattori, H. Yamamoto, J. Am. Chem. Soc.2019141, 12288-12295.

    13. Selective Synthesis of Primary Amines from Nitriles under Hydrogenation Conditions, M. Yoshimura, A. Komatsu, M. Niimura, Y. Takagi, T. Takahashi, S. Ueda, T. Ichikawa, Y. Kobayashi, H. Okami, T. Hattori, Y. Sawama, Y. Monguchi, H. Sajiki, Adv. Synth. Catal., 2018, 360, 1726-1732.

    12. ニッケルを触媒とした臭化アルキル化合物の遠隔位カルボキシル化反応, 服部倫弘, ファルマシア, 2018, 54, 351.

    11. Catalyst-Dependent Selective Hydrogenation of Nitriles: Selective Synthesis of Tertiary and Secondary Amines, Y. Monguchi, M. Mizuno, T. Ichikawa, Y, Fujita, E. Murakami, T. Hattori, T. Maegawa, Y. Sawama, H. Sajiki, J. Org. Chem201782, 10939-10944.

    10. Ruthenium on carbon catalysed carbon-carbon cleavage of aryl alkyl ketones and aliphatic aldehydes in aqueous media, T. Hattori, H. Okami, T. Ichikawa, S. Mori, Y. Sawama, Y. Monguchi, H. Sajiki, Adv. Synth. Catal. 2017359, 3490-3495.

    9. Heterogeneous one-pot carbonylation and Mizoroki–Heck reactions in a parallel manner following the cleavage of cinnamaldehyde derivatives, T. Hattori, S. Ueda, R. Takakura, Y. Sawama, Y. Monguchi, H. Sajiki, Chem. Eur. J201723, 8196-8202; Selected to be highlighted on the ChemistryViews website

    8. Palladium-Catalyzed C-H Monoalkoxylation of α,β-Unsaturated Carbonyl Compounds, Y. Monguchi, K. Kunishima, T. Hattori, T. Takahashi, Y. Shishido, Y. Sawama, H. Sajiki, ACS Catalysis 20166, 3994–3997.

    7. Switching the Cleavage Sites in Palladium on Carbon-Catalyzed Carbon-Carbon Bond Disconnection, T. Hattori, R. Takakura, T. Ichikawa, Y. Sawama, Y. Monguchi, H. Sajiki, J. Org. Chem201681, 2737–2743; Highlighted in Synfacts 2016, 753.

    6. Tertiary-Amino-Functionalized Resin-Supported Palladium Catalyst for the Heterogeneous Suzuki-Miyaura Reaction of Aryl Chlorides, Y. Monguchi, T. Ichikawa, M. Netsu, T. Hattori, T. Mizusaki, Y. Sawama, H. Sajiki, Synlett 201526, 2014–2018.

    5. Facile Arene Hydrogenation under Flow Conditions Catalyzed by Rhodium or Ruthenium on Carbon, T. Hattori, T. Ida, A. Tsubone, Y. Sawama, Y. Monguchi, H. Sajiki, Eur. J. Org. Chem201511, 2492–2497.

    4. Palladium on Carbon-Catalyzed Suzuki-Miyaura Coupling Reaction Using an Efficient and Continuous Flow System, T. Hattori, A. Tsubone, Y. Sawama, Y. Monguchi, H. Sajiki, Catalysts 20155, 18–25.

    3. Systematic evaluation of the palladium-catalyzed hydrogenation under flow conditions, T. Hattori, A. Tsubone, Y. Sawama, Y. Monguchi, H. Sajiki, Tetrahedron 201470, 4790–4798; Highlighted in Synfacts 2014992.

    2. Chemoselective Hydrogenation Catalyzed by Pd on Spherical Carbon, H. Esaki, T. Hattori, A. Tsubone, S. Mibayashi, T. Sakata, Y. Sawama, Y. Monguchi, H. Yasuda, K. Nosaka, H. Sajiki, ChemCatChem 201313, 3629–3635.

    1. Palladium on Carbon-Catalyzed Cross-Coupling Using Triarylbismuths, Y. Monguchi, T. Hattori, Y. Miyamoto, T. Yanase, Y. Sawama, H. Sajiki, Adv. Synth. Catal2012354, 2561–2567.

    Patent

    11. アミド反応用用反応剤及びそれを用いたアミド化合物の製造方法、国際公開番号WO/2021/085635

    10.  アミド反応用用反応剤及びそれを用いたアミド化合物の製造方法、国際公開番号WO/2021/085636

    9. アミド化合物の製造方法、国際公開番号WO/2021/085636

    8. アミド化合物の製造方法、国際公開番号WO/2021/208731

    7. アミド化合物の製造方法、国際公開番号WO/2021/199147

    6. 不均一系パラジウム触媒存在下でアルデヒドを一酸化炭素源として用いるハロゲン化合物のカルボニル化反応によりカルボニル化合物を得る方法ビフェニル化合物の合成法、特許第6871802号

    5. フェノール誘導体の選択的メチル化方法、特許第6871793号

    4. 白金族金属担持触媒及び反応装置、特許第6042278号

    3. 白金族担持型接触水素化還元触媒及び水素化還元方法、特許第6042277号

    2. ビフェニル化合物の合成法、特許第5907006号

    1. ビフェニル化合物の合成法、特許第5907005号