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wise Chemical Reduction of [4]Cyclo[4]helicenylene: Stereo Transformation and Site-Selective Metal Complexation"Z. Zhou, Y. Yang, J. Liang, S. Sato, Z. Zhang, and Z. Wei Precis. Chem. 2024, in press. [10.1021/prechem.4c00064]
"Molecular Cylinders with Donor-Acceptor Structure and Swinging Motion" K. Li, S. Yoshida, R. Yakushiji, X. Liu, C. Ge, Z. Xu, Y. Ni, X. Ma, J. Wu, S. Sato, and Z. Sun Chem. Sci. 2024, in press. [10.1039/D4SC05849F]
"Crystallization-Induced Dimerization and Solution-Phase Bond Dissociation of Stable Dibenzoolympicenyl Radicals"X. Zhang, H. He, C. Ge, Q. Xiang, S. Sato, M. Lv, X. Chen, and Z. Sun Angew. Chem. Int. Ed. 2024, 63, e202418261. [10.1002/anie.202418261]
"Dynamics of Side Chains in Poly(quinoxaline-2,3-diyl)s Studied via Quasielastic Neutron Scattering"R. Inoue, Y. Nagata, T. Tominaga, S. Sato, Y. Kawakita, T. Yamawaki, K. Morishima, M. Suginome, and M. Sugiyama J. Chem. Phys. 2024, 161, 054905. [10.1063/5.0215603]
"Conformational Analysis of (+)-Germacrene D-4-ol Using the Crystalline Sponge Method to Elucidate the Origin of its Instability" Y. Jung, T. Mitsuhashi, K. Kageyama, T. Kikuchi, S. Sato, and M. Fujita Chem. Eur. J. 2024, 30, e202400512. [10.1002/chem.202400512]
"Cyclic Sesquiterpene–Flavanone [4+2] Hybrids, Syzygioblanes A–C, Found in an Indonesian Traditional Medicine, “Jampu Salo” (Syzygium oblanceolatum)" N. Koga, Y. Saito, K. Miyake, S. Amuti, S. Fukuyoshi, S. Yoshida, S. Sato, Y. Yamada, A. Ikeda, N. Adachi, M. Kawasaki, A. Takasu, S. Aramaki, T. Senda, A. Rahim, A. Najib, G. Alam, N. Tanaka, and K. Nakagawa-Goto Org. Lett. 2024, 26, 4302-4307. [10.1021/acs.orglett.4c01248]
"Chiral Inversion of Thalidomide During Crystal Growth by Sublimation"M. Kira, Y. Shiga, K. Nakagawa, A. Matsumoto, K. Tokita, Y. Terasawa, K. Zhang, K. Tsutao, T. Nakanishi, S. Yoshida, S. Sato, N. Shibata, and T. Asahi Cryst. Growth Des. 2024, 24, 3133-3139. [10.1021/acs.cgd.3c01030]
"Rapid Synthesis of Chiral Figure-Eight Macrocycles Using a Preorganized Natural Product-Based Scaffold" T. Honda, D. Ogata, M. Tsurui, S. Yoshida, S. Sato, T. Muraoka, Y. Kitagawa, Y. Hasegawa, J. Yuasa, and H. Oguri Angew. Chem. Int. Ed. 2024, e202318548. [10.1002/anie.202318548]
"Enantioselective Synthesis of 3-(N-Indolyl)Quinolines Containing Axial and Central Chiralities" K. Yamanomoto, K. Yamamoto, S. Yoshida, S. Sato, and T. Akiyama Chem. Commun. 2024, 60, 582-585. [10.1039/D3CC05142K]
"Function and Structure of a Terpene Synthase Encoded in a Giant Virus Genome" Y. Jung, T. Mitsuhashi, S. Sato, M. Senda, T. Senda, and M. Fujita J. Am. Chem. Soc. 2023, 145, 25966-25970. [10.1021/jacs.3c10603]
"Synthesis of (±)-Zeapyranolactone, a Noncanonical Strigolactone Isolated from Maize, and Determination of Its Overall Relative Configuration"C. Ono-Ogasawara, S. Yamamoto, Y. Ogura, H. Okamura, K. Takaba, S. Yoshida, S. Sato, K. Yonekura, and H. Takikawa Tetrahedron Lett. 2023, 127, 154695. [10.1016/j.tetlet.2023.154695]
"X-ray and Electron Diffraction Observations of Steric Zipper Interactions in Metal-Induced Peptide Cross-β Nanostructures"E. Tsunekawa, Y. Otsubo, Y. Yamada, A. Ikeda, N. Adachi, M. Kawasaki, A. Takasu, S. Aramaki, T. Senda, S. Sato, S. Yoshida, M. Fujita, and T. Sawada J. Am. Chem. Soc. 2023, 145, 16160-16165. [10.1021/jacs.3c04710]
"Synthetic Modulation of an Unstable Dehydrosecodine-type Intermediate and Its Encapsulation into a Confined Cavity Enable Its X-ray Crystallographic Observation"G. Tay, T. Wayama, H. Takezawa, S. Yoshida, S. Sato, M. Fujita, and H. Oguri Angew. Chem. Int. Ed. 2023, 62, e202305122. [10.1002/anie.202305122]
"Hysteresis Behavior in the Unfolding/Refolding Processes of a Protein Trapped in Metallo-Cages" T. Nakama, A. Rossen, R. Ebihara, M. Yagi-Utsumi, D. Fujita, K. Kato, S. Sato, and M. Fujita Chem. Sci. 2023, 14, 2910-2914. [10.1039/D2SC05879K]
"Synthesis and Structure Elucidation of Triarylmethyl Radicals with Anthryl Substitution"P. Wang, J. Hu, Z. Xu, Z. Pu, S. Sato, X. Zhang, W. Hu, and Z. Sun Chem. Commun. 2023, 59, 2015-2018. [10.1039/D2CC06083C]
"Photo‑Conversion of Self‑Assembled Structures into Continuous Covalent Structures via [2 + 2]‑Cycloaddition Reactions"M. Inada, A. Udagawa, S. Sato, T. Asahi, and K. Saito. Photochem. Photobiol. Sci. 2022, 21, 2169–2177. [10.1007/s43630-022-00286-0]
"Pentagon-Containing Doublet Graphene Fragments with Edge-Dependent Spin/Charge Distribution"Z. Gong, Q. Xiang, K. Li, Z. Xu, J. Hu, Y. Ni, S. Sato, and Z. Sun. Chin. J. Chem. 2022, 21, 2525-2530. [10.1002/cjoc.202200344]
"Synthesis of a Negatively Curved Nanocarbon Molecule with an Octagonal Omphalos via Design-of-Experiments Optimizations Supplemented by Machine Learning" K. Ikemoto, M. Akiyoshi, T. Mio, K. Nishioka, S. Sato, and H. Isobe Angew. Chem. Int. Ed. 2022, 61, e202204035. [10.1002/anie.202204035]
"Single-Crystal Structure Analysis of Non-Deuterated Triglycine Sulfate by Neutron Diffraction at 20 and 298 K: a New Disorder Model for the 298 K Structure" Y. Terasawa, T. Ohhara, S. Sato, S. Yoshida, and T. Asahi Acta Cryst. 2022, E78, 306-312. [10.1107/S2056989022000858]
"Overcrowded Ethylene-Bridged Nanohoop Dimers: Regioselective Synthesis, Multiconfigurational Electronic States, and Global Hückel/Möbius Aromaticity" K. Li, Z. Xu, J. Xu, T. Weng, X. Chen, S. Sato, J. Wu, and Z. Sun J. Am. Chem. Soc. 2021, 143, 20419-20430. [10.1021/jacs.1c10170]
"Comprehensive Structural Analysis of the Bitter Components in Beer by the HPLC-Assisted Crystalline Sponge Method" Y. Taniguchi, T. Kikuchi, S. Sato, and M. Fujita Chem. Eur. J. 2021, 28, e202103339. [10.1002/chem.202103339]
"Giant Optical Anisotropy in High Temperature Superconducting Cuprate Bi2Sr2CaCu2O8+δ" K. Zhang, M. Matsumoto, K. Nakagawa, A. Matsuda, G. Shino, S. Sato, T. Ikeda, and T. Asahi J. Phys. Soc. Jpn. 2021, 90, 113702. [10.7566/JPSJ.90.113702]
"Cycloparaphenylene Double Nanohoop: Structure, Lamellar Packing, and Encapsulation of C60 in the Solid State" Y. Yang, S. Huangfu, S. Sato, and M. Jurícek Org. Lett. 2021, 23, 7943-7948. [10.1021/acs.orglett.1c02950]
"Cycloparaphenylene–Phenalenyl Radical and Its Dimeric Double Nanohoop" Y. Yang, O. Blacque, S. Sato, and M. Juricek Angew. Chem. Int. Ed. 2021, 60, 13529-13535. [10.1002/anie.202101792]
"Chemical Reduction of a Nanosized [6]Cyclo-2,7-naphthylene Macrocycle"Z. Zhou, Z. Wei, K. Ikemoto, S. Sato, H. Isobe, and M. A. Petrukhina Angew. Chem. Int. Ed. 2021, 60, 11201-11205. [10.1002/anie.202100942]
"Preferences of Polarity and Chirality in Triglycine Sulfate Crystals by Alanine Ghost" Y. Terasawa, T. Kikuta, M. Ichiki, S. Sato, K. Ishikawa, and T. Asahi J. Phys. Chem. Solids 2020, 151, 109890. [10.1016/j.jpcs.2020.109890]
"A Case Study of Stereoisomerism with [6]Cyclo[4]helicenylenes"T. Matsuno, Y. Yang, Y. Nanjo, H. Isobe, and S. Sato Chem. Lett. 2020, 50, 110-112. [10.1246/cl.200717]
"Crystalline Naphthylene Macrocycles Capturing Gaseous Small Molecules in Chiral Nanopores" T. Matsuno, K. Fukunaga, S. Kobayashi, P. Sarkar, S. Sato, T. Ikeda, and H. Isobe Chem. Asian J. 2020, 15, 3829-3835. [10.1002/asia.202000876]
"Synthesis and stereoisomerism of [n]cyclo-2,9-phenanthrenylene congeners possessing alternating E/Z- and R/S-biaryl linkages" Y. Yang, Y. Nanjo, H. Isobe, and S. Sato Org. Biomol. Chem. 2020, 18, 4949-4955. [10.1039/D0OB01064B]
"Ineffective OH Pinning of the Flipping Dynamics of a Spherical Guest within a Tight-Fitting Tube" T. Matsuno, M. Someya, S. Sato, S. Maeda, and H. Isobe Angew. Chem. Int. Ed. 2020, 59, 14570-14576. [10.1002/anie.202005538]
"Acyclic, Linear Oligo-meta-Phenylenes as Multipotent Base Materials for Highly Efficient Single-Layer Organic Light-Emitting Devices" A. Yoshii, Y. Onaka, K. Ikemoto, T. Izumi, S. Sato, H. Kita, H. Taka, and H. Isobe Chem. Asian J. 2020, 15, 2181-2186. [10.1002/asia.202000521]
"A Nitrogen-Doped Nanotube Molecule with Atom Vacancy Defects" K. Ikemoto, S. Yang, H. Naito, M. Kotani, S. Sato, and H. Isobe Nature Commun. 2020, 11, 1807. [10.1038/s41467-020-15662-6]
"Synthesis of a Hemispherical Geodesic Phenine Framework by a Polygon Assembling Strategy" T. Mio, K. Ikemoto, S. Sato, and H. Isobe Angew. Chem. Int. Ed. 2020, 59, 6567-6571. [10.1002/anie.201915509]