文部科学省 新学術領域研究(平成27年~31年)反応集積化が導く中分子戦略:高次生物機能分子の創製

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  • H. Shimoda, T. Shibata, D. Sekine, *M. Nakada, "Synthetic Studies on Keramaphidin B: Formation of a Macrocyclic Ring by Intramolecular Diels-Alder Reaction", Heterocycles, 2020, 100, 3-11
  • M. Uwamori, R. Osada, R. Sugiyama, K. Nagatani, *M. Nakada, "Enantioselective Total Synthesis of Cotylenin A", J. Am. Chem. Soc, 2020, 142, 5556-5561
  • K. Kasama, H. Aoyama, *S. Akai, "Enantiodivergent synthesis of axially chiral biphenyls from σ-symmetric 1,1ʹ-biphenyl-2,6-diol derivatives by single lipase-catalyzed acylative and hydrolytic desymmetrization", Eur. J. Org. Chem., 2020, , 654–661
  • F. Kühn, S. Katsuragi, Y. Oki, C. Scholz, *S. Akai, *H. Gröger, "Dynamic kinetic resolution of a tertiary alcohol", Chem. Comuun., 2020, 56, 2885-2888
  • Cocatalysis. K. Higashio, S. Katsuragi, D. Kundu, N. Adebar, C. Plass, F. Kühn, *H. Gröger, *S. Akai, "Continuous-Flow Dynamic Kinetic Resolution of Racemic Alcohols by Lipase–Oxovanadium", Eur. J. Org. Chem., 2020, , 1961-1967
  • Ichinari, D.;Ashikari,Y. ;Mandai,K.;Aizawa, Y.; Yoshida, J.; Nagaki, A, "A Novel Approach to Functionalization of Aryl Azides via Generation and Reactions of Organolithiums Bearing Masked Azides Using Flow MicroreactorsIchinari", Angew. Chem. Int. Ed. , 59, 1567-1571
  • Baralle, A.; Inukai, T.; Yanagi, T.; Nogi, K.; Osuka, A.; Nagaki, A.*; Yoshida, J.; Yorimitsu, H.*, "Tf2O-mediated Reaction of Alkenyl Sulfoxides with Unprotected Anilines in Flow Microreactors", Chem. Lett. , 49, 160-163
  • Yamamoto, T.; Tonomura, O.; Nagaki, A, "Continuous Production Using a T-shaped Micro/milli-reactor for RUCY-catalyzed AsymmetricHydrogenation of Acetophenone", J. Chem. Eng. Jpn., 53, 73-77
  • Takahashi, Y.; Ashikari, Y.; Takumi, M.; Shimizu, Y.; Jiang, Y.; Higuma, R.; Ishikawa, S.; Sakaue, H.; Shite, I.; Maekawa, K.; Aizawa, Y.; Yamashita, H.; Yonekura, Y.; Colella, M.; Luisi, R.; Takegawa, T.; Fujita, C.; Nagaki, A.*, "Synthesis of Biaryls Having a Piperidylmethyl Group Based on Space Integration of Lithiation,Borylation and Suzuki-Miyaura Coupling. ", Eur. J. Org.Chem., , 618-622
  • A, Cartier, E. Levernier, A-L. Dhimane, *T. Fukuyama, *C. Ollivier, *I. Ryu, *L. Fensterbank, "Synthesis of Aliphatic Amides through a Photoredox Catalyzed Radical Carbonylation Involving Organosilicates as Alkyl Radical, Precursors", Adv. Synth. Catal., 2020, , in press
  • Y. Furukawa, M. Hayashi, S. Hayase, T. Nokami, *T. Itoh, "Visible Light-Driven Direct 2,2-Difluoroacetylation Using Organic Pigment Catalys", ACS Sus. Chem. Eng., 2020, , in press
  • K. Yano, T. Itoh, *T. Nokami, "Total Synthesis of Myc-IV(C16:0, S) via Automated Electrochemical Assembly", Carbohydr. Res., 2020, 492, 108018
  • *K. Mitsudo, R. Matsuo, T. Yonezawa, H. Inoue, H. Mandai, *S. Suga, "Electrochemical Synthesis of Thienoacene Derivatives: Transition Metal-Free Dehydrogenative C-S Coupling Promoted by a Halogen Mediator.", Angew. Chem., Int. Ed., , in press
  • *Omori, M. Nakayama, H. Mandai, S. Yamamoto, H. Kobayashi, H. Sako, K. Sakaida, H. Yoshimura, S. Ishii, S. Ibaragi, K. Hirai, K. Yamashiro, T. Yamamoto, S. Suga, S. Takashiba, "The Fungal Metabolite (+)-Terrein Abrogates Osteoclast Differentiation via Suppression of the RANKL Signaling Pathway through NFATc1.", Int. Immunopharmacol., , in press
  • T. Sugahara, A. E. Ferao, A. Rey, J. Guo, S. Aoyama, K. Igawa, K. Tomooka, *T. Sasamori, D. Hashizume, S. Nagase, N. Tokitoh, "1,2-Insertion Reactions of Alkynes into Ge-C Bonds of Arylbromogermylene", Dalton Trans. , 2020, , in press
  • A. M. Jeckel, K. Matsumura, K. Nishikawa, Y. Morimoto, R. A. Saporito, T. Grant, *D. R. Ifa, "Use of Whole-Body Cryosectioining and Desorption Electrospray Ionization Mass Spectrometry Imaging (DESI-MSI) To Visualize Alkaloid Distribution in Poison Frogs", J. Mass Spectrom., 2020, 55, in press
  • K. Adachi, T. Yamada, H. Ishizuka, M. Oki, S. Tsunogae, N. Shimada, O. Chiba,T. Orihara, M. Hidaka, T. Hirokawa, M. Odagi, K. Konoki, M. Y. Yamashita, *K. Nagasawa, "Synthesis of C12-keto saxitoxin derivatives with unusual inhibitory activity against voltage-gated sodium channels. ", Chem. Eur. J., 2020, 26, 2025-2033
  • M. Odagi, K. Okuda, H. Ishizuka, K. Adachi, *K. Nagasawa, "Synthesis of Spiroguanidine Derivatives by Dearomative Oxidative Cyclization using Hypervalent Iodine Reagent.", Asian J. Org. Chem., 2020, 9, 218-221
  • Y. Hidaka, N. Kiya, M. Yoritate, K. Usui, G. Hirai, "Synthesis of CH2-linked α-galactosylceramide and its glucose analogues through glycosyl radical-mediated direct C-glycosylation", Chem. Commun., , in press
  • Y. Hayashi, Y. Ishigaki, J. Merad, T. Suzuki, M. Médebielle, "5-Arylidenetetronate as a Versatile Electrophore for Pi-Extended Electron Acceptors", Heterocycles, 2020, , in press
  • Y. Ishigaki, T. Harimoto, K. Sugimoto, L. Wu, W. Zeng, D. Ye, T. Suzuki, "Hexaarylbutadiene: a versatile scaffold with tunable redox properties towards organic near-infrared electrochromic material", Chem. Asian J. , 2020, 15, 1147-1155
  • Y. Ishigaki, T. Hashimoto, K. Sugawara, S. Suzuki, T. Suzuki, "Switching of Redox Properties Triggered by a Thermal Equilibrium between Closed-shell Folded and Open-shell Twisted Species.", Angew. Chem. Int. Ed. , 2020, 59, 6581-6584
  • L. Wu, Y. Ishigaki, Y. Hu, K. Sugimoto, W. Zeng, T. Harimoto, Y. Sun, J. He, T. Suzuki, X. Jiang, H.-Y. Chen, D. Ye, "H2S-activatable near-infrared afterglow luminescent probes for sensitive molecular imaging in vivo.", Nat. Commun., 2020, 11, 446
  • K. Sugawara, W. Nojo, Y. Ishigaki, J. Ohkanda, T. Suzuki, "A Novel Condensed Heterocyclic Quinone with a Dibezofuranobisthiadiazole Skeleton", Heterocycles , 2020, 101, 99-103
  • T. Saito, K. Fujiwara, Y. Sano, T. Sato, Y. Kondo, U. Akiba, Y. Ishigaki, R. Katoono, T. Suzuki, "An improved synthesis of the C42-C52 segment of ciguatoxin 3C.", Tetrahedron Lett. , 2018, 59, 1372-1376
  • 服部春香、松本光、星野友、三浦佳子*, "有機分子触媒L-prolineを固定化した多孔質高分子モノリスの開発およびフロー不斉Aldol付加反応への応用", 化学工学論文集, 2020, , in press
  • N. Sugisawa, H. Nakamura, and *S. Fuse, "Micro-flow synthesis of β-amino acid derivatives via a rapid dual activation approach", Chem. Commun., 2020, , in press
  • Y. Otake, Y. Shibata, Y. Hayashi, S. Kawauchi, H. Nakamura, and S. Fuse, "N-Methylated peptide synthesis via acyl N-methylimidazolium cation generation accelerated by a Brønsted acid", Angew. Chem. Int. Ed., 2020, , in press
  • Y. Minami, K. Nishida, *A. Konishi, *M. Yasuda, "Characterization of Highly Coordinated Allylgermanes: Pivotal Players for Enhanced Nucleophilicity and Stereoselectivity", Chem. Asian. J., 2020, , in press
  • J. Matsuoka, S. Inuki, Y. Matsuda, Y. Miyamoto, M. Otani, M. Oka, S. Oishi, *H. Ohno, "Total Synthesis of Dictyodendrins A–F by the Gold-Catalyzed Cascade Cyclization of Conjugated Diyne with Pyrrole", Chem. Eur. J., 2020, 26(49), 11150–11157
  • T. Fukuda, M. Nagatomo, *M. Inoue, "Total Synthesis of Diospyrodin and Its Three Diastereomers", Org. Lett., 2020, 22(16), 6468–6472
  • H. Fujino, T. Fukuda, M. Nagatomo, *M. Inoue, "Convergent Total Synthesis of Hikizimycin Enabled by Intermolecular Radical Addition to Aldehyde", J. Am. Chem. Soc., 2020, 142(30), 13227−13234
  • *A. Konishi, Shoya Satake, *M. Yasuda, "Catalytic Cycloisomerization of Conjugated Bisbutatrienes into Pentalene Skeletons: Synthesis and Properties of Bisbutatrienes with an Acenaphthene Backbone", Chem. Lett., 2020, 49(5), 589-592
  • *M. Kumagai, K. Nishikawa, T. Mishima, I. Yoshida, M. Ide, A. Watanabe, K. Fujita, Y. Morimoto, "Fluorinated Kavalactone Inhibited RANKL-Induced Osteoclast Differentiation of RAW264 Cells", Biol. Pharm. Bull., 2020, 43(5), 898–903
  • Y. Arai, S. Torigoe, T. Matsumaru, S. Yamasaki, *Y. Fujimoto, "The key entity of a DCAR agonist, phosphatidylinositol mannoside Ac1PIM1: its synthesis and immunomodulatory function", Org. Biomol. Chem.,
  • *M. Inoue, Y. Sumii, *N. Shibata, "Contribution of Organofluorine Compounds to Pharmaceuticals", ACS Omega, 2020, , in press
  • K. Niina, K. Tanagawa, Y. Sumii, N. Saito, *N. Shibata, "Pyridine tetrafluoro-λ6-sulfanyl chlorides: Spontaneous addition to alkynes and alkenes in the presence or absence of photo-irradiation", Org. Chem. Front. , 2020, , in press
  • *Y. Nishimoto, *M. Yasuda, "Carbometalation and Heterometalation of Carbon-Carbon Multipl-Bonds Using Group-13 Heavy Metals: Carbogallation, Carboindation, Heterogallation, and Heteroindation", Chem. Asian. J., 2020, 15(6), 636-650
  • Y. Hioki, A. Mori, *K. Okano, "Steric effects on deprotonative generation of cyclohexynes and 1,2-cyclohexadienes from cyclohexenyl triflates by magnesium amides", Tetrahedron, 2020, 76(na), in press
  • K. Igawa, Y. Kawasaki, S. Nozaki, N. Kokan, *K. Tomooka, "Ozone Oxidation of Silylalkene: Mechanistic Study and Application for the Synthesis of Silacarboxylic Acid Derivatives", J. Org. Chem. , 2020, 85, 4165-4171
  • H. Watanabe, M. Takemoto, K. Adachi, Y. Okuda, A. Dakegata, T. Fukuyama, I. Ryu, K. Wakamatsu, *A. Orita, "Syntheses of Diarylethenes by Perylene-catalyzed Photodesulfonylation from Ethenyl Sulfones", Chem. Lett., 49(4), pp. 409?412
  • R. Masuda, Y. Kawasaki, K. Igawa, Y. Manabe, H. Fujii, N. Kato, K. Tomooka, *J. Ohkanda, "Copper-Free Huisgen Cycloaddition for the 14-3-3-Templated Synthesis of Fusicoccin-Peptide Conjugates", Chem. Asian. J. , 2020, 17, 742-747
  • H. Uno, N. Punna, E. Tokunaga, M. Shiro, *N. Shibata, "Synthesis of Both Mirror Images of 9-Membered CF3-Heterocycles using a Single Antipode of Chiral Ligand under Pd-catalyzed Decarboxylative Ring-expansion with Kinetic Resolution", Angew. Chem., Int. Ed. , 2020, , in press
  • J. Kishi, S. Inuki, E. Kashiwabara, T. Suzuki, N. Dohmae, *Y. Fujimoto, "Design and Discovery of Covalent α-GalCer Derivatives as Potent CD1d Ligands", ACS Chem. Biol., 15(2), 353-359
  • N. Sugisawa, Y. Otake, H. Nakamura, and *S. Fuse, "Single-step, rapid, and mild synthesis of -amino acid N-carboxy anhydrides using micro-flow technology", Chem. Asian J., 2020, 15(1), 79-84
  • Y. Hosoya, I. Kobayashi, K. Mizoguchi, *M. Nakada, "Palladium-Catalyzed Carbothiolation via Trapping of the σ‑Alkyl Palladium Intermediate with RSTIPS", Org. Lett., 2019, 21, 8280-8284
  • Y. Sato, Y. Hosoya, I. Kobayashi, K. Adachi, *M. Nakada, "Preparation of a Chiral Building Block by an Organocatalytic Asymmetric Intramolecular Michael Reaction", Asian J. Org. Chem. , 2019, 8, 1033-1036
  • *M. N. Uddin, Z. A. Siddique, N. Mase, M. Uzzaman, W. Shumi, "Oxotitanium(IV) complexes of some bis-unsymmetric Schiff bases: Synthesis, structural elucidation and biomedical applications", Appl. Organomet. Chem., 2019, 33, e4876
  • R. Ide, R. Kyan, T. Phuc Le, Y. Kitagawa, K. Sato, N. Mase, *T. Narumi, "Chemoselective Umpolung of Enals for Asymmetric Homoenolate Cross-Annulation of Enals and Aldehydes Catalyzed by N-Heterocyclic Carbene", Org. Lett., 2019, 21, 9119-9123
  • *N. Mase, Moniruzzaman; S. Yamamoto, K. Sato, T. Narumi, H. Yanai, "Epimerization-suppressed organocatalytic synthesis of poly-L-lactide in supercritical carbon dioxide under plasticizing conditions", Tetrahedron Lett., 2019, 60, 150987
  • *K. Takeda, N. Yanagi, K. Nonaka, N. Mase, "Estimation of Outlet Temperature of a Flow Reactor Heated by Microwave Irradiation", Chem. Rec., 2019, 19, 140-145
  • P. Vamosi, K. Matsuo, T. Masuda, K. Sato, T. Narumi, *K. Takeda, *N. Mase, "Rapid Optimization of Reaction Conditions Based on Comprehensive Reaction Analysis Using a Continuous Flow Microwave Reactor", Chem. Rec., 2019, 19, 77-84
  • A. Matsumoto, *K. Asano, *S. Matsubara, "Kinetic Resolution of Acylsilane Cyanohydrins via Organocatalytic Cycloetherification.", Chem.—Asian J., 2019, 14, 116–120
  • Y. Kato, C. M. Williams, M. Uchiyama, S. Matsubara, "A Protocol for an Iodine–Metal Exchange Reaction on Cubane Using Lithium Organozincates", Org. Lett., 2019, 21, 473–475
  • Y. Kurimoto, T. Nasu, Y. Fujii, *K. Asano, *S. Matsubara, "Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers.", Org. Lett., 2019, 21, 2156-2160
  • A. Matsumoto, *K. Asano, *S. Matsubara, "Organocatalytic Enantio- and Diastereoselective Construction of syn-1,3-Diol Motifs via Dynamic Kinetic Resolution of In Situ Generated Chiral Cyanohydrins.", Org. Lett. , 2019, 21, 2688-2692
  • S. Teranishi, K. Maeda, *T. Kurahashi, *S. Matsubara, "Diastereoselective Synthesis of 1,3-Oxazolidines via Cationic Iron Porphyrin-catalyzed Cycloaddition of Aziridines with Aldehydes.", Org. Lett., 2019, 21, 2593-2596
  • A. Matsumoto, *K. Asano, *S. Matsubara, "Asymmetric syn-1,3-Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts", Asian J. Org. Chem. , 2019, 8, 814-818
  • R. Tomifuji, S. Masuda, *T. Kurahashi, *S. Matsubara, "Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes", Org. Lett., 2019, 21, 3834-3837
  • R. Tomifuji, *T. Kurahashi, *S. Matsubara, "Asymmetric Aza‐Diels–Alder Reaction with Ion‐Paired – Iron Lewis Acid – Brønsted Acid Catalyst.", Chem.–Eur. J. , 2019, 25, 8987-8991
  • K. Maeda, *T. Kurahashi, *S. Matsubara, "Chlorotrifluoromethylation of Terminal Olefins by Atom Transfer‐Type Radical Reaction Catalyzed by Cobalt Complexes", E. J. Org. Chem., 2019, , 4623-4626
  • T. Inami, T. Takahashi, *T. Kurahashi, *S. Matsubara, "ickel-Catalyzed [5+2] Cycloaddition of 10π-Electron Aromatic Benzothiophenes with Alkynes To Form Thermally Metastable 12πElectron Nonaromatic Benzothiepines.", J. Am. Chem. Soc., 2019, 141, 12541-12544
  • Y. Wada, A. Matsumoto, *K. Asano, *S. Matsubara, "Enantioselective bromination of axially chiral cyanoarenes in the presence of bifunctional organocatalysts.", RSC Adv., 2019, 9, 31654-31658
  • M. Noshita, Y. Shimizu, H. Morimoto, S. Akai, Y. Hamashima, N. Ohneda, H. Odajima, *T. Ohshima, "Ammonium Salt-Accelerated Hydrazinolysis of Unactivated Amides: Mechanistic Investigation and Application to a Microwave Flow Process", Org. Process Res. Dev., 2019, 23, 588–594
  • Endo, Y.; Furusawa, M.; Shimazaki, T.; Takahashi, Y.; Nakahara, Y.; Nagaki, A., "Molecular Weight Distribution of Polymers Produced by Anionic Polymerization Enables Mixability Evaluation", Org. Process Res. Dev., 23, 635-640
  • Nakahara, Y.; Metten, B.; Tonomura, O.; Nagaki, A.; Hasebe, S.; Yoshida, J., "Modeling and Design of Flow Microreactor-based Process for Synthesizing Ionic Liquids", Org. Process Res. Dev., 23, 641-647
  • Nagaki, A.; Sasatsuki, K.; Ishiuchi, S.; Miuchi, N.; Takumi, M.; Yoshida, J., "Synthesis of Functionalized Ketones from Acid Chlorides and Organolithiums by Extremely Fast Micromixing", Chem. Eur. J., 25, 4946-4950
  • Nagaki, A.; Yamashita, H.; Hirose, K.; Tsuchihashi, Y.; Yoshida, J, "Alkyllithium Compounds Bearing Electrophilic Functional Groups: A Flash Chemistry Approach", Angew. Chem., Int. Ed., 58, 4027-4030
  • Nagaki, A.; Hirose, K.; Mitamura, K.; Matsukawa, K.; Ishizuka, N.; Yamamoto, T.; Takumi, M.; Takahashi, Y.; Yoshida, J, "Suzuki-Miyaura Coupling Using Monolithic Pd Reactors and Scaling-up by Series Connection of the Reactors ", Catalyst,, 9(300), 1月24日
  • Tonomura, O.; Taniguchi, S.; Nishi, K.; Nagaki, A.; Hirose, K.; Yoshida, J.; Ishizuka, N.; Hasebe, S., " Blockage Detection and Diagnosis of Externally Parallelized Monolithic Microreactors ", Catalyst,, 9(308), 1月12日
  • Hori, M.; Nogi, K.; Nagaki, A.; Yorimitsu, H., "Annulative Synthesis of Thiazoles and Oxazoles from Alkenyl Sulfoxides and Nitriles via Additive Pummerer Reaction", Asian J. Org. Chem., 8, 1084-1087
  • Nagaki, A.; Jiang, Y.; Yamashita, H.; Takabayashi, N.;Yoshida, J., "Monolithiation of 5,5’-Dibromo-2,2’-bithiophene Using Flow Microreactors. Mechanistic Implications and Synthetic Applications.", Chem. Eng. Tech. , 42, 2113-2118
  • Takahashi, Y.; Nagaki, A.*, "Anionic Polymerizations using Flow Microreactors. ", Molecules, 24, 1532
  • Nakahara, Y.; Furusawa, M.; Endo, Y.; Shimazaki, T.; Takahashi, Y.; Jiang, Y.; Nagaki, A., "Practical Continuous Flow Controlled/Living Anionic Polymerization. ", Chem. Eng. Tech., 42, 2154-2163
  • Nagaki, A.*, "Recent Topics of Functionalized Organolithiums using Flow Microreactor Chemistry", Tetrahedron Lett., 60, 150923
  • Nagaki, A.; Yamashita, H.; Hirose, K.; Tsuchihashi, Y.; Takumi, M.; Yoshida, "Generation and Reaction of Functional Alkyllithiums Using Microreactors and Their Application to Heterotelechelic Polymer Synthesis", J. Chem. Eur. J., 25, 13719-13727
  • Ashikari, Y.; Saito,K.; Nokami, T.; Yoshida, J.; Nagaki, A. , " Oxo-Thiolation of Cationically Polymerizable Alkenes Using Flow Microreactors", Chem. Eur. J. , 25, 15239-15243
  • Colella, M.; Nagaki, A.*; Luisi, R.*, "Flow Technology for Genesis and Use of (Highly) Reactive Organometallic Reagents ", Chem. Eur. J., 26, 19-32
  • Mandai, K.; Tsuchihashi, Y.; Ashikari, Y.; Yoshida, J.; Nagaki, A.*, "18O-Labeled chiral compounds enable the facile determination of enantioselectivity by massspectroscopy. ", Tetrahedron Lett., 61, 151367
  • M. Kono, *S. Harada, T. Nozaki, Y. Hashimoto, S. Murata, H. Gröger, Y. Kuroda, K. Yamada, K. Takasu, Y. Hamada, *T. Nemoto, "Asymmetric Formal Synthesis of (+)-Catharanthine via Desymmetrization of Isoquinuclidine", Org. Lett., 2019, 21, 3750–3754
  • Y. Mogi, K. Inanaga, H.Tokuyama, M. Ihara, Y. Yamaoka, K. Yamada, *K. Takasu, "Rapid Assembly of Protoilludane Skeleton through Tandem Catalysis: Total Synthesis of Paesslerin A and Its Structural Revision", Org. Lett., 2019, 21, 3954–3958
  • T. Ito, M. Tsutsumi, K. Yamada, H. Takikawa, Y. Yamaoka, *K. Takasu, "Synthesis of Functionalized Medium-Sized trans-Cycloalkenes by 4π Electrocyclic Ring Opening– Alkylation Cascade", Angew. Chem. Int. Ed., 2019, 58, 11836-11840
  • K. Shimoda, Y. Yamaoka, D. Yoo, K. Yamada, H. Takikawa, *K. Takasu, "Total Syntheses of Allelopathic 4-Oxyprotoilludanes, Melleolides and Echinocidins", J. Org. Chem., 2019, 84, 11014-11024
  • N. Ogawa, Y. Yamaoka, H. Takikawa, *K. Takasu, "Synthesis of Polycyclic Spirocarbocyles via Acid-Promoted Ring-Contraction/Dearomative Ring-Closure Cascade of Oxapropellanes", Org. Lett., 2019, 21, 7563-7567
  • S. Ishida, K.Terayama, R. Kojima, K. Takasu, *Y. Okuno, "Prediction and Interpretable Visualization of Retrosynthetic Reactions Using Graph Convolutional Networks", J. Chem. Inf. Model., 2019, 59, 5026-5033
  • H. Watanabe, M. Takemoto, K. Adachi, Y. Okuda, A. Dakegata, T. Fukuyama, I. Ryu, K. Wakamatsu, *A. Orita, "Syntheses of Diarylethenes by Perylene-catalyzed Photodesulfonylation from Ethenyl Sulfones", Chem. Lett. , 2020, 49, 409-412
  • T. Fukuyama, T. Nishikawa, *I. Ryu, "Site-Selective C(sp3)–H Functionalization of Fluorinated Alkanes Driven by Polar Effects Using a Tungstate Photocatalyst, ", Eur. J. Org. Chem., 2020, 2020, 1424 – 1428
  • *M. Ueda, M. Hayama, H. Hashishita, A. Munechika, Aiko, T. Fukuyama, "Controlled [3+2] and [2+2] Cycloadditions of 1,3-Bifunctional Allenes with C60 by Using a Flow Reaction System,", Eur. J. Org. Chem., 2019, 2019, 6764-6769
  • M. Uno, S. Sumino, T. Fukuyama, M. Matsuura, Y. Kuroki, Y. Kishikawa, *I. Ryu, "Synthesis of 4,4-Difluoroalkenes by Coupling of α Substituted α,αDifluoromethyl Halides with Allyl Sulfones under Photoredox Catalyzed Conditions", J. Org. Chem., 2019, 84, 9330 – 9338
  • T. Fukuyama, T. Kippo, K. Hamaoka, *I. Ryu, "Br-radical-mediated [3+2] Annulation: Synthesis of 2-Bromomethylsubstituted Alkenylcyclopentanes by the Reaction of Alkenylcyclopropanes with Allyl Bromides under Photo irradiation", Sci. China Chem., 2019, 62, 1525 – 1528
  • T. Fukuyama, T. Okada, N. Nakashima, *I. Ryu, "Radical Mediated Aza-Pauson-Khand Reaction of Acetylenes, Imines, and CO Leading to Five-Membered Unsaturated Lactams", Helv. Chim. Acta, , 2019, 102, e1900186
  • M. Ueda, A. Maeda, K. Hamaoka, M. Sasano, T. Fukuyama, *I. Ryu, "Bromine-Radical-Mediated Site-Selective Allylation of C(sp3)-H Bonds", Synthesis , 2019, 51, 1171 – 1177
  • Y. Kondo, H. Morimoto, *T. Ohshima, "Recent Progress towards the Use of Benzophenone Imines as an Ammonia Equivalent", Chem. Lett., 2020, 49, 497–504
  • Y. Isoda, K. Kitamura, S. Takahashi, *T. Nokami, *T. Itoh, "Mixed-Electrolytes-Driven Stereoselective Electrochemical Glycosylation", ChemElectroChem, 2019, 6, 4149-4152
  • Y. Masuhara, T. Tanaka, H. Takenaka, S. Hayase, T. Nokami, *T. Itoh, "Synthesis of gem-Difluoromethylene Containing Cycloalkenes via Ring-opening Reaction of gem-Difluorocyclopropanes and Subsequent RCM Reaction", J. Org. Chem., 2019, 84, 5540-5449
  • K. Yamaguchi, H. Usui, Y. Domi, H. Nishida, T. Komura, T. Nokami, T. Itoh, *H. Sakaguchi, "Electrochemical performance of Sn4P3 negative electrode for Na-ion batteries in ether-substituted ionic liquid electrolyte", J. Electroanal. Chem., 2019, 845, 66-71
  • S. Manmode, S. Tanabe, T. Yamamoto, N. Sasaki, *T. Nokami, *T. Itoh , "Electrochemical Glycosylation as an Enabling Tool for the Stereoselective Synthesis of Cyclic Oligosaccharides ", ChemistryOpen, 2019, 8, 869-872
  • Y. Ashikari, K. Saito, T. Nokami, *J. Yoshida, *A. Nagaki, "Oxo‐Thiolation of Cationically Polymerizable Alkenes Using Flow Microreactors", Chem. Eur. J., 2019, 25, 15239-15243
  • Y. Domi, H. Usui, A. Ueno, Y. Shindo, H. Mizuguchi, T. Komura, T. Nokami, T. Itoh, *H. Sakaguchi, "Effect of Annealing Temperature of Ni-P/Si on its Lithiation and Delithiation Properties", J. Electrochem. Soc., 2020, 167, 040512
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特許

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  • 平井剛、深澤亮、袖岡幹子, 理化学研究所, シアル酸誘導体, 特願2016-147705, 2016年7月27日, 2018年2月1日
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