・Ishihara, K. et al. (2021) A Fluorous Proline Catalyst Immobilized on Teflon® for Highly Stereoselective Asymmetric Aldol Reactions. Heterocycles, 103, 839-861.
・Ishihara, K. et al. (2020) An Expeditious Approach to Tetrazoles from Amides Utilizing Phosphorazidates. Org. Lett., 22, 6244-6247.
・Ishihara, K. et al. (2020) A recyclable and highly stereoselective multi-fluorous proline catalyst for asymmetric aldol reactions. Tetrahedron Lett., 61, 151657.
・Ishihara, K. et al. (2020) SNAr azidation of phenolic functions utilizing diphenyl phosphorazidate. Tetrahedron Lett., 61, 151493.
・Ishihara, K. et al. (2019) Stereospecific Synthesis of 1,5-Disubstituted Tetrazoles from Ketoximes via a Beckmann Rearrangement Facilitated by Diphenyl Phosphorazidate. Tetrahedron Lett., 60, 1295-1298.
・Kobayashi, Y. et al. (2019) Unprecedented Asymmetric Epoxidation of Isolated Carbon–Carbon Double Bonds by a Chiral Fluorous Fe(III) Salen Complex: Exploiting Fluorophilic Effect for Catalyst Design. Eur. J. Org. Chem., 2401-2408.
・Kobayashi, Y. et al. (2018) Activation of Grubbs-Hoveyda second-generation Catalysts Employing Aromatic Ligands Bearing a Widespread Aryl Substituent. Heterocycles, 97, 806-822.
・ 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.
・ Sugiyama, Y. et al. (2017) Fluorous Mixture Synthesis of Tripeptides and Pentapeptides using a Fluorous-Fmoc Protection Strategy. Synthesis, 49, 2187-2204.
・ Kobayashi, Y. 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.