・Kobayashi, Y. et al. (2018) Activation of Grubbs-Hoveyda second-generation Catalysts Employing Aromatic Ligands Bearing a Widespread Aryl Substituent. Heterocycles, in press.
・ Ishihara, K. et al. (2018) A Practical Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes employing Azide Anion from Diphenyl Phosphorazidate. Synthesis, 50, 1293-1300.
・ Ishihara, K. et al. (2017) Pummerer Rearrangement using Bis(p-nitrophenyl) Phosphorazidate as an Azidation Reagent: A Novel Synthesis of Azidomethyl Sulfides. Tetrahedron Lett., 58, 3932-3935.
・ Matsugi, M. (2017) Concise Synthesis of Peptide Analogs Using a Fluorous -Fmoc Protection strategy. In New Horizons of Process Chemistry Scable Reactions and Technologies; K. Tomioka, T. Shioiri, H. Sajiki, Eds.; Springer Nature, pp201-215.
・ Matsugi, M. et al. (2017) Fluorous Mixture Synthesis of Tripeptides and Pentapeptides using a Fluorous-Fmoc Protection Strategy. Synthesis, 49, 2187-2204.
・ Matsugi, M. et al. (2017) Grubbs–Hoveyda 2nd generation catalysts activated by the introduction of a light fluorous tag onto the bidentate ligands. Synthesis, 49, 1796-1807.
・ Matsugi, M. et al. (2016) Highly activated second-generation Grubbs–Hoveyda catalyst driven by intramolecular steric strain. Synlett, 27, 2352-2356.
・ Ishihara, K. et al. (2016) Synthesis of 5-Substituted 1H-Tetrazoles from Aldoximes Using Diphenyl Phosphorazidate. Synlett, 27, 2225-2228.
・ Matsugi, M. et al. (2015) Development of Efficient Processes for Multi-gram Scale and Divergent Preparation of Fluorous-Fmoc Reagents. Tetrahedron, 71, 4958-4966.
・ Matsugi, M. et al. (2015) Concise Synthesis of All Stereoisomers of Dendroamide A by Fluorous Mixture Synthesis Based on Fluorous-Fmoc Protection of Amino Acids. Eur. J. Org. Chem., 3971-3982.
・ Matsugi, M. et al. (2015) A medium fluorous Grubbs-Hoveyda 2nd generation catalyst for phase transfer catalysis of ring closing metathesis reactions. Tetrahedron Lett., 56, 1363-1366.
・ Shioiri, T. et al. (2015) SN2 displacement at the quaternary carbon center: A novel entry to the synthesis of α,α-disubstituted α-amino acids. Tetrahedron Lett., 56, 3169-3171.
・ Amii, H. et al. (2015) Enhancement of stereoselectivities in asymmetric synthesis using fluorinated solvents, auxiliaries, and catalysts. RSC Adv., 5, 17269-17282.