業績リスト

原著論文(2008年以降)

  • S. Saito, M. Ishida, Y. Busujima, M. Ebihara, K. Kohama, N. Tanaka, E. Toya, M. Nakamura, T. Kanamori, T. Furuta, S. Matsumoto, S. Karasawa, H. Yuasa, and T. Hata, “Magnesium-Promoted Benzidine-Type Rearrangement for Regioselective Construction of Polyfunctionalized Biaryls.” Chem. Eur. J., e03607 (2026).
  • K. Abe, K. Nishi, H. Ito, S. Kobayashi, S. Saito, and T. Hata, “Iron/NHC-Catalyzed Regio- and Stereoselective 1,6-Additions of Aliphatic Grignard Reagents to α,β,γ,δ-Unsaturated Carbonyl Compounds: Asymmetric Variants with Chiral NHCs.” Angew. Chem. Int. Ed., e18346 (2025).
  • S. Kikukawa, M. Ebihara, K. Kobayashi, N. Kasakura, T. Kanamori, T. Furuta, A. Kohata, N. Funahashi, S. Matsumoto, S. Karasawa, K. Kinbara, N. Koshikawa, H. Yuasa, and T. Hata, “Facile Synthesis of 5-Halo-1,2,3-triazole-fused Benzotricyclic Frameworks from 1-(ω-Azidoalkyl)-2-(2,2-dihalovinyl)arenes and their Application in Fluorescent Triazole Derivatives.” Eur. J. Org. Chem., 28, e202500355 (2025).
  • T. Hata, K. Nishi, K. Yamaguchi, Y. Tatsumi, N. Tanaka, M. Shigeta, and H. Urabe, “Copper-Catalyzed Reductive Coupling of Nitroalkanes with Aliphatic Grignard/Cerium and Organozinc Reagents for Synthesis of Functionalized Nitrones.” Adv. Synth. Catal., 367, e202401259 (2025).
  • D. Sekita, H. Fujita, Y. Mizuno, T. Horii, T. Hata, and T. Fujie, “Facile Coating of Low-molecular-weight Stretchable Adhesive Films Leveraging Carbodiimide-to-urea Conversion and Gallic Acid for Enhanced Adhesion.” Mater. Adv., 6, 1513-1519 (2025).
  • T. Hata, K. Nishi, D. Goto, Y. Tatsumi, M. Shigeta, and H. Urabe, “Iron-Catalyzed Reductive Coupling of Nitro Compounds with Grignard and Organozinc Reagents for Synthesis of Functionalized Secondary Amines.” Adv. Synth. Catal., 367, e202401034 (2025).
  • S. Kobayashi, K. Abe, and T. Hata, “Iron-N,N,N’,N’-Tetramethylethylenediamine-Catalyzed Selective Substitution of Functionalized Diene and Triene Monoepoxides with Aliphatic Grignard Reagents.” Adv. Synth. Catal., 366, 5183-5189 (2024).
  • T. Hata, Y. Tatsumi, Y. Kanai, N. Takahashi, M. Shigeta, and H. Urabe, “Preparation of Hetero-π-conjugated Compounds by Double Nucleophilic Addition to Haloalkynes and C-H Cyclization.” Adv. Synth. Catal., 366, 2136-2140 (2024).
  • A. Ishii, T. Hata, Y. Shigeta, and H. Urabe, “Nucleophilic Addition of Amides to Haloalkynes: Synthesis of (Z)-β-Halovinylamides as Dual Precursors of Allyl Halides and Alkylidene Carbenes.” Org. Lett., 26, 2999-3003 (2024).
  • T. Abe, K. Kobayashi, S. Kikukawa, Y. Kanai, and T. Hata, “Rhodium-Catalyzed Intramolecular Cyclization and Rearrangement of 1-Azido-2-(2,2-Dihalovinyl)arenes and 1-Azido-2-[(2,2-Dihalovinyl)(Boc)amino]arenes for the Preparation of 2,3-Dihaloindoles and 2-Haloquinoxalines.” Adv. Synth. Catal., 365, 4562-4566 (2023).
  • K. Kobayashi, N. Kasakura, S. Kikukawa, S. Matsumoto, S. Karasawa, and T. Hata, “Facile Preparation of Polycyclic Halogen-substituted 1,2,3-Triazoles by Using Intramolecular Huisgen Cycloaddition.” Org. Biomol. Chem., 21, 9610-9615 (2023).
  • K. Miyanaka, T. Harada, M. Shigeta, T. Hata, and H. Urabe, “Iron-catalyzed Regio- and Stereoselective Substitution of 2,4-Alkadienyl Carboxylates with Aryl Grignard Reagents.” Tetrahedron Lett., 133, 154824 (2023).
  • T. Hata, Y. Hayashi, Y. Hasegawa, M. Iwai, A. Ishii, M. Hasegawa, M. Shigeta, and H. Urabe, “Preparation of Tetrazole-fused π-Conjugated Molecules and Their Fluorescence Behavior,” Chem. Lett., 48, 662-665 (2019).
  • G. Sugano, K. Kawada, M. Shigeta, T. Hata, and H. Urabe, “Iron-catalyzed δ-Selective Conjugate Addition of Methyl and Cyclopropyl Grignard Reagents to α,β,γ,δ-Unsaturated Carbonyl Compounds,” Tetrahedron Lett., 60, 885-890 (2019).
  • A. Furukawa, T. Hata, M. Shigeta, and H. Urabe, “Rh-catalyzed Intramolecular Cyclization of N-Sulfonyltriazole and Sulfinate. Concise Preparation of Sulfonylated Unsaturated Piperidines,” Tetrahedron Lett., 60, 815-819 (2019).
  • M. Senoo, A. Furukawa, T. Hata, and H. Urabe, “Rh-catalyzed Intramolecular C-H Bond Activation with Triazoles. Preparation of Stereo-defined Pyrrolidines and Other Related Cyclic Compounds,” Chem. Eur. J., 22, 890-895 (2016).
  • M. Yamagishi, A. Ishii, T. Hata, and H. Urabe, “Facile Preparation of 1,2-Dihydroisoquinolines from N-Benzylsulfonamides and Bromoacetylenes,” Heterocycles, 90, 847-856 (2015). (Current Special Issue: Isao Kuwajima’s Special Issues)
  • T. Mizumori, T. Hata, and H. Urabe, “Alkylation of Pyridines at Their 4-Position with Stylenes plus an Yttrium Reagent or Benzyl Grignard Reagents,” Chem. Eur. J., 21, 422-426 (2015).
  • H. Murase, K. Senda, M. Senoo, T. Hata, and H. Urabe, “Rhodium-catalyzed Intramolecular Hydroarylation of 1-Halo-1-alkynes. Regioselective Synthesis of Semihydrogenated Aromatic Heterocycles,” Chem. Eur. J., 20, 317-322 (2014).
  • T. Hata, H. Gotoh, T. Yokomizo, and H. Urabe, “Iron-catalyzed 1,6-Selective Addition of Aryl Grignard Reagent to tert-Butyl (Z)-5-Phenyl-3-hexenoate,” Org. Synth., 91, 307-321 (2014).
  • T. Hata, T. Nakada, O. Y. Taek, N. Hirone, and H. Urabe, “Iron-Catalyzed Regio- and Stereoselective Conjugate Addition of Aryl Grignard Reagents to α,β,γ,δ-Unsaturated Sulfones and Its Synthetic Application,” Adv. Synth. Catal., 355, 1736-1740 (2013).
  • S. Iwata, M. Senoo, T. Hata, and H. Urabe, “Preparation of S-Aryl Arenethiosulfonates from N,N-Di(arenesulfonyl)hydrazines. Reduction of Sulfonyl Chlorides with an Organic Reagent,” Heteroat. Chem., 24, 336-344 (2013).
  • M. Yamagishi, K. Nishigai, A. Ishii, T. Hata, and H. Urabe, “Facile Preparation of Indoles and 1,2-Benzothiazine 1,1-Dioxides via Nucleophilic Addition of Sulfonamides to Bromoacetylenes Followed by Pd-Catalyzed Cyclization,” Angew. Chem. Int. Ed., 51, 6471-6474 (2012).
  • T. Hata, H. Imade, and H. Urabe, “Four Nucleophilic Additions to Alkenynedioic Acid Derivatives in Tandem; Efficient One-pot Synthesis of Bicyclo[4.2.0]octenols,” Org. Lett., 14, 2450-2453 (2012).
  • M. Yamagishi, K. Nishigai, A. Ishii, T. Hata, and H. Urabe, “Nucleophilic Addition of Sulfonamides to Bromoacetylenes: Facile Preparation of Pyrroles,” Org. Lett., 14, 34-37 (2012).
  • T. Hata, S. Iwata, S. Seto, and H. Urabe, “Iron-Catalyzed Synthesis of Allenes from 2-Alken-4-ynoates and Grignard Reagents” Adv. Synth. Catal. 354, 1885-1889 (2012).
  • T. Hata, S. Sujaku, N. Hirone, K. Nakano, J. Imoto, H. Imade, and H. Urabe, “Iron-Mediated and -Catalyzed Metallative Cyclization of Electron Withdrawing Group-substituted Alkynes and Alkenes with Grignard Reagents,” Chem.-Eur. J., 17, 14593-14602 (2011).
  • Y. T. Oh, K. Senda, T. Hata, and H. Urabe, “Rh-catalyzed Intramolecular Debenzylative Cyclization of Amines. Butyrolactams from Benzylamines Having a Chloroacetylene Moiety,” Tetrahedron Lett., 52, 2458-2461 (2011).
  • N. Hirone, H. Sanjiki, R. Tanaka, T. Hata, and H. Urabe, “Acceleration of the Substitution of Silanes with Grignard Reagents by Using either LiCl or YCl3/MeLi,” Angew. Chem. Int. Ed., 49, 7762-7764 (2010).
  • Y. Kato, D. H. Yen, T. Hata, and H. Urabe, “Aryl(sulfonyl)amino Group: A Convenient and Stable yet Activated Modification of Amino Group for Its Intramolecular Displacement,” Org. Lett., 12, 4137-4139 (2010).
  • H. Naito, T. Hata, and H. Urabe, “Selective Deprotection of Methanesulfonamides to Amines,” Org. Lett., 12, 1228-1231 (2010).
  • T. Hata, R. Bannai, M. Otsuki, and H. Urabe, “Iron-Catalyzed Regio- and Stereoselective Substitution of γ,δ-Epoxy-α,β-unsaturated Esters and Amides with Grignard Reagents,” Org. Lett., 12, 1012-1014 (2010).
  • D. Shikanai, H. Murase, T. Hata, and H. Urabe, “Rh-catalyzed Isomerization and Intramolecular Redox Reaction of Alkynyl Ethers Affording Dihydropyrans and Ketoolefins,” J. Am. Chem. Soc., 131, 3166-3167 (2009).
  • T. Hata, N. Hirone, S. Sujaku, K. Nakano, and H. Urabe, “Iron-Mediated Intramolecular Metallative Cyclization of α,β-Unsaturated Esters and Amides. Versatile One-Pot Preparation of Bicyclic Ketoesters,”Org. Lett.,10, 5031-5033 (2008).
  • S. Okada, K. Arayama, R. Murayama, T. Ishizuka, K. Hara, N. Hirone, T. Hata, and H. Urabe, “Iron-Catalyst-Switched Selective Conjugate Addition of Grignard Reagents. α,β,γ,δ-Unsaturated Amides as Versatile Templates for Asymmetric Three-Component Coupling Process,” Angew. Chem. Int. Ed., 47, 6860-6864 (2008). † Equal contribution
  • Y. Fukudome, H. Naito, T. Hata, and H. Urabe, “Copper-Catalyzed 1,2-Double Amination of 1-Halo-1-alkynes. Concise Synthesis of Protected Tetrahydropyrazines and Related Heterocyclic Compounds,” J. Am. Chem. Soc., 130, 1820-1821 (2008).
  • H. Naito, T. Hata, and H. Urabe, “Facile Preparation of N-Protected 2-Alkylidene-1,3-imidazolidines,” Tetrahedron Lett., 49, 2298-3201 (2008).

総説等(2009年以降)

  • T. Hata, “Synthetic Methods Using Interaction Between Sustainable Iron Reagent and Functionalized Carbon-Carbon Multiple Bonds,” in Molecular Technology, (Volume 4: Synthesis Innovation) Yamamoto, H, Kato, T, Eds., Wiley-VCH, pp. 51-76 (2019).
  • 秦、”鉄試薬による官能性炭素−炭素多重結合の制御を利用する新規合成手法の開発”、有機合成化学協会誌、72, 972-982 (2014).
  • 占部、秦、”第4章 芳香族化合物 – 医薬品化学への展開”、生命理工系のための大学院基礎講座 – 有機化学、湯浅英哉・編、東京工業大学出版会・工学図書、pp. 67-90 (2011).
  • 占部、秦、”バイオ研究のフロンティア 医療・診断をめざす先端バイオテクノロジー3、(13章 医薬・生体機能分子の未来指向型合成法の開発)”関根光雄・編、東京工業大学出版会・工学図書、pp. 118-130 (2009).