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Specially Appointed Associate Professor
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nagata atmark

MAEDA, Satoshi Group
Principal Investigator
Faculty Members
Postdoctoral Fellows

About the Research

Research History

See my CV.

Representative Research Achievements

  • Asymmetric Catalysis in Chiral Solvents: Chirality Transfer with Amplification of Homochirality through a Helical Macromolecular Scaffold
    Nagata, R. Takeda, M. Suginome, ACS Cent. Sci., 2019, 5, 1235-1240
    DOI: 10.1021/acscentsci.9b00330
  • Elucidating the Solvent Effect on the Switch of the Helicity of Poly(quinoxaline-2,3-diyl)s: A Conformational Analysis by Small-Angle Neutron Scattering
    Nagata, T. Nishikawa, M. Suginome, S. Sato, M. Sugiyama, L. Porcar, A. Martel, R. Inoue, N. Sato, J. Am. Chem. Soc., 2018, 140, 2722-2726
    DOI: 10.1021/jacs.7b11626
  • Poly(quinoxaline-2,3-diyl) as a Multifunctional Chiral Scaffold for Circularly Polarized Luminescent Materials: Color Tuning, Energy Transfer, and Switching of the CPL Handedness
    Nishikawa, Y. Nagata, M. Suginome, ACS Macro Lett., 2017, 6, 431-435
    DOI: 10.1021/acsmacrolett.7b00131
  • Poly(quinoxaline-2,3-diyl)s Bearing (S)-3-Octyloxymethyl Side Chains as an Efficient Amplifier of Alkane Solvent Effect Leading to Switch of Main-Chain Helical Chirality
    Nagata, T. Nishikawa, M. Suginome, J. Am. Chem. Soc., 2014, 136, 15901-15904
    DOI: 10.1021/Ja509531t
  • Solid Polymer Films Exhibiting Handedness-Switchable, Full-Color-Tunable Selective Reflection of Circularly Polarized Light
    Nagata, K. Takagi, M. Suginome, J. Am. Chem. Soc., 2014, 136, 9858-9861
    DOI: 10.1021/ja504808r

Related Research



  • Atroposelective Total Synthesis of Cihunamide B
    L. H. Yu, Y. Nagata, H. Nakamura, J. Am. Chem. Soc., 2024, 146, 4, 2549-2555
    DOI: 10.1021/jacs.3c11016


  • OSPAR: A Corpus for Extraction of Organic Synthesis Procedures with Argument Roles
    K. Machi, S. Akiyama, Y. Nagata, M. Yoshioka, J. Chem. Inf. Model., 2023, 63, 21, 6619-6628
    DOI: 10.1021/acs.jcim.3c01449
  • Microfluidic Platform Using Focused Ultrasound Passing through Hydrophobic Meshes with Jump Availability
    Y. Koroyasu, T. V. Nguyen, S. Sasaguri, A. Marzo, I. Ezcurdia, Y. Nagata, T. Yamamoto, N. Nomura, T. Hoshi, Y. Ochiai, T. Fushimi, Pnas Nexus, 2023, 2, 7, pgad207
    DOI: 10.1093/pnasnexus/pgad207
  • Synthesis and Chiroptical Properties of Binaphthyl-Hinged [5]Helicenes
    M. Hasegawa, Y. Nojima, Y. Nagata, K. Usui, K. I. Sugiura, Y. Mazaki, European Journal of Organic Chemistry, 2023, ,
    DOI: 10.1002/ejoc.202300656
  • Diastereoselective Rotaxane Synthesis with Pillar 5 Arenes via Co-Crystallization and Solid-State Mechanochemical Processes
    K. Wada, K. Yasuzawa, S. X. Fa, Y. Nagata, K. Kato, S. Ohtani, T. Ogoshi, J. Am. Chem. Soc., 2023, 145, 28, 15324–15330
    DOI: 10.1021/jacs.3c02919
  • Synthesis of Cationic Azatriphenylene Derivatives by Electrochemical Intramolecular Pyridination and Characterization of Their Optoelectronic Properties
    Y. Ohno, S. Ando, D. Furusho, R. Hifumi, Y. Nagata, I. Tomita, S. Inagi, Org. Lett., 2023, ,
    DOI: 10.1021/acs.orglett.3c01341
  • Amino-Ene Click Reaction of Electron-Deficient Pi-Conjugated Molecules with Negative Activation Enthalpies
    H. Sanematsu, Y. Nagata, M. Takeuchi, A. Takai, Chem. Eur. J., 2023, ,
    DOI: 10.1002/chem.202301019
  • Adaptive Planar Chirality of Pillar[5]arenes Invertible by n-Alkane Lengths
    K. Adachi, S. Fa, K. Wada, K. Kato, S. Ohtani, Y. Nagata, S. Akine, T. Ogoshi, J. Am. Chem. Soc., 2023, 145, 8114-8121
    DOI: 10.1021/jacs.3c01019
  • Highly Chemoselective Ligands for Suzuki-Miyaura Cross-Coupling Reaction Based on Virtual Ligand-Assisted Screening
    W. Matsuoka, Y. Harabuchi, Y. Nagata, S. Maeda, Org. Biomol. Chem., 2023, 21, 3132-3142
    DOI: 10.1039/d3ob00398a
  • Aggregation-Induced Circularly Polarized Phosphorescence of Pt(ii) Complexes with an Axially Chiral BINOL Ligand
    D. Tauchi, T. Koida, Y. Nojima, M. Hasegawa, Y. Mazaki, A. Inagaki, K. I. Sugiura, Y. Nagaya, K. Tsubaki, T. Shiga, Y. Nagata, H. Nishikawa, Chem. Commun., 2023, 27,
    DOI: 10.1039/d2cc06198h
  • Predicting Highly Enantioselective Catalysts Using Tunable Fragment Descriptors
    N. Tsuji, P. Sidorov, C. D. Zhu, Y. Nagata, T. Gimadiev, A. Varnek, B. List, Angew. Chem., Int. Ed., 2023, ,
    DOI: 10.1002/anie.202218659
  • TEtraQuinolines: A Missing Link in the Family of Porphyrinoid Macrocycles
    W. Xu, Y. Nagata, N. Kumagai, J. Am. Chem. Soc., 2023, 145, 4, 2609–2618
    DOI: 10.1021/jacs.2c12582


  • Discrete Chiral Organic Nanotubes by Stacking Pillar 5 Arenes Using Covalent Linkages
    T. H. Shi, S. Fa, Y. Nagata, K. Wada, S. Ohtani, K. Kato, T. Ogoshi, Cell Reports Physical Science, 2022, 3,
    DOI: 10.1016/j.xcrp.2022.101173
  • A Twisted Chiral Cavitand with 5-Fold Symmetry and Its Length- Selective Binding Properties
    T. H. Shi, Y. Nagata, S. Akine, S. Ohtani, K. Kato, T. Ogoshi, J. Am. Chem. Soc., 2022, 144, 51, 23677–23684
    DOI: 10.1021/jacs.2c11225
  • Real-Time Chirality Transfer Monitoring from Statistically Random to Discrete Homochiral Nanotubes
    S. X. Fa, T. H. Shi, S. Akama, K. Adachi, K. Wada, S. Tanaka, N. Oyama, K. Kato, S. Ohtani, Y. Nagata, S. Akine, T. Ogoshi, Nat. Commun., 2022, 13, Article number: 7378
    DOI: 10.1038/s41467-022-34827-z
  • A Semi-Automated Material Exploration Scheme to Predict the Solubilities of Tetraphenylporphyrin Derivatives
    R. Shirasawa, I. Takemura, S. Hattori, Y. Nagata, Communications Chemistry, 2022, 5, Article number: 158 (2022)
    DOI: 10.1038/s42004-022-00770-9
  • Quantum Chemical Calculations to Trace Back Reaction Paths for the Prediction of Reactants
    Y. Sumiya, Y. Harabuchi, Y. Nagata, S. Maeda, Jacs Au, 2022, 2, 1181-1188
    DOI: 10.1021/jacsau.2c00157
  • Preparative-Scale Synthesis of Nonacene
    A. Jancarik, J. Holec, Y. Nagata, M. Samal, A. Gourdon, Nat. Commun., 2022, 13,
    DOI: 10.1038/s41467-021-27809-0
  • Synthesis, Structure, and Dynamics of Chiral Eight-Membered Cyclic Molecules with Thienylene and Cyclopropylene Units Alternately Connected
    T. Miura, Y. Ishihara, T. Nakamuro, S. Moritani, Y. Nagata, M. Murakami, Chem. Eur. J., 2022, 28,
    DOI: 10.1002/chem.202103962
  • Young Career Focus: Professor Yuuya Nagata (Hokkaido University, Sapporo, Japan)
    Y. Nagata, Synlett, 2022, 33, A3-A4
    DOI: 10.1055/s-0040-1720546


  • Cyclodextrins with Multiple Pyrenyl Groups: An Approach to Organic Molecules Exhibiting Bright Excimer Circularly Polarized Luminescence
    H. Shigemitsu, K. Kawakami, Y. Nagata, R. Kajiwara, S. Yamada, T. Mori, T. Kida, Angew. Chem., Int. Ed., 2021, 61,
    DOI: 10.1002/anie.202114700
  • Alkali Metal Fluorides in Fluorinated Alcohols: Fundamental Properties and Applications to Electrochemical Fluorination
    N. Shida, H. Takenaka, A. Gotou, T. Isogai, A. Yamauchi, Y. Kishikawa, Y. Nagata, I. Tomita, T. Fuchigami, S. Inagi, J. Org. Chem., 2021, 86, 16128-16133
    DOI: 10.1021/acs.joc.1c00692
  • Tyrosine-Based Photoluminescent Diketopiperazine Supramolecular Aggregates
    N. Shimosaraya, T. Sotani, Y. Miyagi, E. A. Q. Mondarte, K. Suthiwanich, T. Hayashi, Y. Nagata, H. Sogawa, F. Sanda, Soft Matter, 2021, 18, 137-145
    DOI: 10.1039/d1sm01206a
  • Protected Amino Acids as a Nonbonding Source of Chirality in Induction of Single-Handed Screw-Sense to Helical Macromolecular Catalysts
    S. Ikeda, R. Takeda, T. Fujie, N. Ariki, Y. Nagata, M. Suginome, Chem. Sci., 2021, ,
    DOI: 10.1039/d1sc01764k
  • Synthesis and Absorption Properties of Long Acenoacenes
    A. Jancarik, D. Mildner, Y. Nagata, M. Banasiewicz, J. Olas, B. Kozankiewicz, J. Holec, A. Gourdon, Chem. Eur. J., 2021, 27, 12388-12394
    DOI: 10.1002/chem.202101577
  • Pre-Regulation of the Planar Chirality of Pillar 5 Arenes for Preparing Discrete Chiral Nanotubes
    S. X. Fa, K. Adachi, Y. Nagata, K. Egami, K. Kato, T. Ogoshi, Chem. Sci., 2021, 12, 3483-3488
    DOI: 10.1039/d1sc00074h
  • A Large Starphene Comprising Pentacene Branches
    J. Holec, B. Cogliati, J. Lawrence, A. Berdonces-Layunta, P. Herrero, Y. Nagata, M. Banasiewicz, B. Kozankiewicz, M. Corso, D. G. Oteyza, A. Jancarik, A. Gourdon, Angew. Chem., Int. Ed., 2021, 60, 7752-7758
    DOI: 10.1002/anie.202016163
  • Stereo- and Enantioselective Synthesis of Propionate-Derived Trisubstituted Alkene Motifs
    T. Miura, N. Oku, Y. Shiratori, Y. Nagata, M. Murakami, Chem. Eur. J., 2021, 27, 3861-3868
    DOI: 10.1002/chem.202004930
  • Regioselective 1,3-Dipolar Cycloaddition of Nitriles with Nitrile Imines Generated from Tetrazoles
    T. Miura, K. Hagiwara, T. Nakamuro, Y. Nagata, N. Oku, M. Murakami, Chem. Lett., 2021, 50, 131-135
    DOI: 10.1246/cl.200634


  • Chiral Macrocycles HavingC(3)Symmetry Resulting from Orientation of Thiophene Rings
    T. Miura, T. Nakamuro, Y. Ishihara, Y. Nagata, M. Murakami, Angew. Chem., Int. Ed., 2020, 59, 20475-20479
    DOI: 10.1002/anie.202009781
  • Holding of Planar Chirality of Pillar 5 Arene by Kinetic Trapping Using Host-Guest Interactions with Achiral Guest Solvents
    Y. Nagata, M. Suzuki, Y. Shimada, H. Sengoku, S. Nishida, T. Kakuta, T. A. Yamagishi, M. Suginome, T. Ogoshi, Chem. Commun., 2020, 56, 8424-8427
    DOI: 10.1039/d0cc03413d
  • Irreverent Nature of Dissymmetry Factor and Quantum Yield in Circularly Polarized Luminescence of Small Organic Molecules
    Y. Nagata, T. Mori, Frontiers in Chemistry, 2020, 8, 6
    DOI: 10.3389/fchem.2020.00448
  • Cubane Chirality via Substitution of a "Hidden" Regular Tetrahedron
    N. Yoshino, Y. Kato, T. Mabit, Y. Nagata, C. M. Williams, M. Harada, A. Muranaka, M. Uchiyama, S. Matsubara, Org. Lett., 2020, 22, 4083-4087
    DOI: 10.1021/acs.orglett.0c01142