Publications

The Fujita Laboratory > Publications

Publications

Find:    sorting:    

2017

  • Application of the Crystalline Sponge Method to Revise the Structure of the Phenalenone Fuliginone
    R. Brkljača, B. Schneider, W. Hidalgo, F. Otálvaro, F. Ospina, S. Lee, M. Hoshino, M. Fujita, S. Urban
    Molecules 2017, 22, 211. [ 10.3390/molecules22020211 ]
  • Cycloelatanene A and B: Absolute Configuration Determination and Structural Revision by the Crystalline Sponge Method
    S. Lee, M. Hoshino, M. Fujita, S. Urban
    Chem. Sci. 2017, 8, 1547-1550. [ 10.1039/c6sc04288k ]
  • Finding a New Crystalline Sponge from a Crystallographic Database
    Y. Inokuma, K. Matsumura, S. Yoshioka, M. Fujita
    Chem. Asian J. 2017, 12, 208-211. [ 10.1002/asia.201601551 ]
  • Permeable Self-Assembled Molecular Containers for Catalyst Isolation Enabling Two-Step Cascade Reactions
    Y. Ueda, H. Ito, D. Fujita, M. Fujita
    J. Am. Chem. Soc. 2017, 139, 6090-6093. [ 10.1021/jacs.7b02745 ]
  • Hyper-Assembly of Self-Assembled Glycoclusters Mediated by Specific Carbohydrate–Carbohydrate Interactions
    G. Yan, T. Yamaguchi, T. Suzuki, S. Yanaka, S. Sato, M. Fujita, K. Kato
    Chem. Asian J. 2017, 12, 968-972. [ 10.1002/asia.201700202 ]
  • Structural Elucidation of Trace Amounts of Volatile Compounds Using the Crystalline Sponge Method
    N. Zigon, T. Kikuchi, J. Ariyoshi, Y. Inokuma, M. Fujita
    Chem. Asian J. 2017, 12, 1057-1061. [ 10.1002/asia.201700515 ]
  • Porous Peptide Complexes by a Folding-and-Assembly Strategy
    T. Sawada, M. Yamagami, S. Akinaga, T. Miyaji, M. Fujita
    Chem. Asian J. 2017, 12, 1715-1718. [ 10.1002/asia.201700458 ]
  • Self-Assembly of a Peptide [2]Catenane through Ω-Loop Folding
    T. Sawada, Y. Inomata, M. Yamagami, M. Fujita
    Chem. Lett. 2017, 46, 1119-1121. [ 10.1246/cl.170438 ]
  • Absolute Configuration Determination by the Crystalline Sponge Method
    S. Sairenji, S. Lee, M. Fujita
    J. Synth. Org. Chem., Jpn. 2017, 75, 538-547. [ 10.5059/yukigoseikyokaishi.75.538 ]
  • Determination of the Absolute Configuration of Compounds Bearing Chiral Quaternary Carbon Centers Using the Crystalline Sponge Method
    S. Sairenji, T. Kikuchi, M. A. Abozeid, S. Takizawa, H. Sasai, Y. Ando, K. Ohmatsu, T. Ooi, M. Fujita
    Chem. Sci. 2017, 8, 5132-5136. [ 10.1039/C7SC01524K ]
  • Chiral Crystalline Sponges for the Absolute Structure Determination of Chiral Guests
    K.-K. Yang, R. Dubey, T. Arai, Y. Inokuma, M. Fujita
    J. Am. Chem. Soc. 2017, 139, 11341-11344. [ 10.1021/jacs.7b06607 ]
  • Enantioselective Synthesis of Tetrahydrocyclopenta[b]indole Bearing a Chiral Quaternary Carbon Center via Pd(II)–SPRIX-Catalyzed C–H Activation
    M.A. Abozeid, S. Sairenji, S. Takizawa, M. Fujita, H. Sasai
    Chem. Commun. 2017, 53, 6887-6890. [ 10.1039/C7CC03199H ]
  • X-Ray Structure Analysis of N-Containing Nucleophilic Compounds by the Crystalline Sponge Method
    F. Sakurai, A. Khutia, T. Kikuchi, M. Fujita
    Chem. Eur. J. 2017, , in press. [ 10.1002/chem.201704176 ]

2016

  • Compressed Corannulene in a Molecular Cage
    B. M. Schmidt, T. Osuga, T. Sawada, M. Hoshino, M. Fujita
    Angew. Chem. Int. Ed. 2016, 55, 1561-1564. [ 10.1002/anie.201509963 ]
  • Capsule-Capsule Conversion by Guest Encapsulation
    S. Wang, T. Sawada, K. Ohara, K. Yamaguchi, M. Fujita
    Angew. Chem. Int. Ed. 2016, 55, 2063-2066. [ 10.1002/anie.201509278 ]
  • Determination of the Absolute Configuration of the Pseudo-Symmetric Natural Product Elatenyne by the Crystalline Sponge Method
    S.Urban, R. Brkljača, M. Hoshino, S. Lee, M. Fujita
    Angew. Chem. Int. Ed. 2016, 55, 2678-2682. [ 10.1002/anie.201509761 ]
  • The Crystalline Sponge Method Updated
    M. Hoshino, A. Khutia, H. Xing, Y. Inokuma, M. Fujita
    IUCrJ 2016, 3, 139-151. [ 10.1107/S2052252515024379 ]
  • In Situ Observation of Thiol Michael Addition to a Reversible Covalent Drug in a Crystalline Sponge
    V. Duplan, M. Hoshino, W. Li, T. Honda, M. Fujita
    Angew. Chem. Int. Ed. 2016, 16, 4919-4923. [ 10.1002/anie.201509801 ]
  • Undeniable Confirmation of the syn-Addition Mechanism for Metal-Free Diboration using the Crystalline Sponge Method
    A. B. Cuenca, V. Duplan, N. Zigon, M. Hoshino, M. Fujita, E. Fernández
    Chem. Eur. J. 2016, 22, 4723-4726. [ 10.1002/chem.201600392 ]
  • Structure Determination of Microbial Metabolites by the Crystalline Sponge method
    Y. Inokuma, T. Ukegawa, M. Hoshino, M, Fujita
    Chem. Sci. 2016, 7, 3910-3913. [ 10.1039/C6SC00594B ]
  • Peptide [4]Catenane by Folding and Assembly
    T. Sawada, M. Yamagami, K. Ohara, K. Yamaguchi, M. Fujita
    Angew. Chem. Int. Ed. 2016, 55, 4519-4522. [ 10.1002/anie.201600480 ]
  • Astellifadiene: Structure Determination by an NMR-Coupled Crystalline Sponge Method and Elucidation of its Biosynthesis
    Y. Matsuda, T. Mitsuhashi, S. Lee, M. Hoshino, T. Mori, M. Okada, H. Zhang, F. Hayashi, M. Fujita, I. Abe
    Angew. Chem. Int. Ed. 2016, 55, 5785-5788. [ 10.1002/anie.201601448 ]
  • A Saccharide-Based Crystalline Sponge for Hydrophilic Guests
    G.-H. Ning, K. Matsumura, Y. Inokuma, M. Fujita
    Chem. Commun. 2016, 52, 7013-7015. [ 10.1039/C6CC03026B ]
  • Self-Assembly of M30L60 Icosidodecahedron
    D. Fujita, Y. Ueda, S. Sato, H. Yokoyama, N. Mizuno, T. Kumasaka, M. Fujita
    Chem 2016, 1, 91-101. [ 10.1016/j.chempr.2016.06.007 ]
  • X-ray Structure Analysis of Ozonides by the Crystalline Sponge Method
    S. Yoshioka, Y. Inokuma, V. Duplan, R. Dubey, M. Fujita
    J. Am. Chem. Soc. 2016, 138, 10140-10142. [ 10.1021/jacs.6b05817 ]
  • Capsule–Bowl Conversion Triggered by a Guest Reaction
    S. Wang, T. Sawada, M. Fujita
    Chem. Commun. 2016, 52, 11653-11656. [ 10.1039/C6CC06551A ]
  • Selective Co-Encapsulation Inside an M6L4 Cage
    S. H. A. M. Lenders, R. Becker, T. Kumpulainen, B. de Bruin, T. Sawada, T. Kato, M. Fujita, J. N. H. Reek
    Chem. Eur. J. 2016, 22, 15468-15474. [ 10.1002/chem.201603017 ]
  • High-Resolution X-ray Structure of Methyl Salicylate, a Time-Honored Oily Medicinal Drug, Solved by Crystalline Sponge Method
    M. Kawahata, S. Komagawa, K. Ohara, M. Fujita, K. Yamaguchi
    Tetrahedron Lett. 2016, 57, 4633-4636. [ 10.1016/j.tetlet.2016.09.017 ]
  • Self-Assembly of Tetravalent Goldberg Polyhedra from 144 Small Components
    D. Fujita, Y. Ueda, S. Sato, N. Mizuno, T. Kumasaka, M. Fujita
    Nature 2016, 540, 563-566. [ 10.1038/nature20771 ]

2015

  • Geometrically Restricted Intermediates in the Self-Assembly of an M12L24 Cuboctahedral Complex
    D. Fujita, H. Yokoyama, Y. Ueda, S. Sato, M. Fujita
    Angew. Chem. Int. Ed. 2015, 54, 155-158. [ 10.1002/anie.201409216 ]
  • Self-Assembled, π-Stacked Complex as a Finely-Tunable Magnetic Aligner for Biomolecular NMR Applications
    S. Sato, R. Takeuchi, M. Yagi-Utsumi, T. Yamaguchi, Y. Yamaguchi, K. Kato and M. Fujita
    Chem. Comm 2015, 51, 2540-2543. [ 10.1039/C4CC09354B ]
  • One-Step Synthesis of [16]Helicene
    K. Mori, T. Murase, M. Fujita
    Angew. Chem. Int. Ed. 2015, 54, 6847-6851. [ 10.1002/anie.201502436 ]
  • Rectifying Electron-Transport Properties through Stacks of Aromatic Molecules Inserted into a Self-Assembled Cage
    S. Fujii, T. Tada, Y. Komoto, T. Osuga, T. Murase, M. Fujita, M. Kiguchi
    J. Am. Chem. Soc. 2015, 137, 5939-5947. [ 10.1021/jacs.5b00086 ]
  • Absolute Structure Determination of Compounds with Axial and Planar Chirality Using the Crystalline Sponge Method
    S. Yoshioka, Y. Inokuma, M. Hoshino, T. Sato, M. Fujita
    Chem. Sci. 2015, 6, 3765-3768. [ 10.1039/C5SC01681A ]
  • Halogen-Bond-Assisted Guest Inclusion in a Synthetic Cavity
    H. Takezawa, T. Murase, G. Resnati, P. Metrangolo, M. Fujita
    Angew. Chem. Int. Ed. 2015, 54, 8411-8414. [ 10.1002/anie.201500994 ]
  • Cavity-Directed Chromism of Phthalein Dyes
    H. Takezawa, S. Akiba, T. Murase, M. Fujita
    J. Am. Chem. Soc. 2015, 137, 7043-7046. [ 10.1021/jacs.5b03618 ]
  • Self-Assembled Spherical Complex Displaying a Gangliosidic Glycan Cluster Capable of Interacting with Amyloidogenic Proteins
    S. Sato, Y. Yoshimasa, D. Fujita, M. Yagi-Utsumi, T. Yamaguchi, K. Kato, M. Fujita
    Angew. Chem. Int. Ed. 2015, 54, 8435-8439. [ 10.1002/anie.201501981 ]
  • Where is the Oxygen? Structural Analysis of a-Humulene Oxidation Products by the Crystalline Sponge Method
    N. Zigon, M. Hoshino, S. Yoshioka, Y. Inokuma, M. Fujita
    Angew. Chem. Int. Ed. 2015, 54, 9033-9037. [ 10.1002/anie.201502302 ]
  • Bridging Adhesion of a Protein onto an Inorganic Surface Using Self-Assembled Dual-Functionalized Spheres
    S. Sato, M. Ikemi, T. Kikuchi, S. Matsumura, K. Shiba, and M. Fujita
    J. Am. Chem. Soc. 2015, 137, 12890-12896. [ 10.1021/jacs.5b06184 ]
  • Cavity-Promoted Diels-Alder Reactions of Unsubstituted Naphthalene: Fine Reactivity Tuning by Cavity Shrinkage
    Y. Fang, T. Murase, M. Fujita
    Chem. Lett. 2015, 44, 1095-1097. [ 10.1246/cl.150351 ]
  • Finely Resolved Threshold for the Sharp M12L24/M24L48 Structural Switch in Multi-Component MnL2n Polyhedral Assemblies: X-ray, MS, NMR, and Ultracentrifugation Analyses
    H. Yokoyama, Y. Ueda, D. Fujita, S. Sato, M Fujita
    Chem. Asian J. 2015, 10, 2292-2295. [ 10.1002/asia.201500519 ]
  • Fitting Proteins into Metal Organic Frameworks
    D. Fujita, M. Fujita
    ACS Cent. Sci. 2015, 1, 352-353. [ 10.1021/acscentsci.5b00315 ]
  • Phosphine-Catalyzed β,γ-Umpolung Domino Reaction of Allenic Esters: Facile Synthesis of Tetrahydrobenzofuranones Bearing a Chiral Tetrasubstituted Stereogenic Carbon Center
    S. Takizawa, K. Kishi, Y. Yoshida, S. Mader, F. Arteaga, S. Lee, M. Hoshino, M. Rueping, M. Fujita, H. Sasai
    Angew. Chem. Int. Ed. 2015, 54, 15511-15515. [ 10.1002/anie.201508022 ]