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2010年以前の研究業績

総説

  • エクステリアフロンティア軌道広がりモデル－ジアステレオ面選択性予測のための試み

    • 友田修司, 金野大助
    有機化学合成協会誌, 2001, 59, 219-231.
    DOI: https://doi.org/10.5059/yukigoseikyokaishi.59.219

原著論文

  • Intramolecular titanium-promoted deoxygenative cyclization to 9-substituted-1,2,3,4-tetrahydrofluorene skeleton

    • Kiyooka, S.; Matsumoto, S.; Umezu, S.; Fujiyama, R.; Kaneno, D.
    Tetrahedron Lett., 2010, 51, 1651-1653.
    DOI: https://doi.org/10.1016/j.tetlet.2009.12.090

  • Theoretical Study on the Mechanism and Diastereoselectivity of NaBH4 Reduction

    • Suzuki, Y.; Kaneno, D.; Tomoda.
    J. Phys. Chem. A., 2009, 113, 2578-2583.
    DOI: https://doi.org/10.1021/jp809966u

  • The Danishefsky Pyranone Puzzle. An Explanation based on the Exterior Frontier Orbital Extension Model

    • Kaneno, D.; Tomoda, S.
    Tetrahedron Lett., 2009, 50, 329-332.
    DOI: https://doi.org/10.1016/j.tetlet.2008.11.004

  • The Importance of Lone Pair Delocalizations: Theoretical Investigations on the Stability of cis and trans Isomers in 1,2-Halodiazenes

    • Yamamoto, T.; Kaneno, D.; Tomoda, S.
    J. Org. Chem., 2008, 73, 15429-5435.
    DOI: https://doi.org/10.1021/jo8006896

  • Solvent effects on the diastereoselection in LiAlH4 reduction of α-substituted ketones

    • Suzuki, Y.; Kaneno, D.; Miura, M.; Tomoda, S.
    Tetrahedron lett., 2008, 49, 4223-4226.
    DOI: https://doi.org/10.1016/j.tetlet.2008.05.002

  • The Origin of Cis-Effect in 1,2-Dihaloethenes: The Quantitative Comparison of Electron Delocalizations and Steric Exchange Repulsions

    • Yamamoto, T.; Kaneno, D.; Tomoda, S.
    Bull. Chem. Soc. Jpn., 2008, 81, 1415-1422.
    DOI: https://doi.org/10.1246/bcsj.81.1415

  • The Importance of Lone Pair Electron Delocalization in the cis-trans Isomers of 1,2-Dibromoethenes

    • Yamamoto, T.; Kaneno, D.; Tomoda, S.
    Chem. lett., 2005, 34, 1190-1191.
    DOI: https://doi.org/10.1246/cl.2005.1190

  • Origin of facial diastereoselection in 2-adamantyl cations. Theoretical evidence against the Felkin-Anh and the Cieplak models

    • D. Kaneno, S. Tomoda
    Tetrahedron lett., 2004, 45, 4559-4562.
    DOI: https://doi.org/10.1016/j.tetlet.2004.04.036

  • Origin of diastereoselection in the hydrosilylation of chiral N-acyliminium intermediates derived from pyroglutamic acid

    • M. Oba, S. Koguchi, K. Nishiyama, D. Kaneno, S. Tomoda
    Angew. Chem. Int. Ed., 2004, 43, 2412-2415.
    DOI: https://doi.org/10.1002/anie.200353366

  • Origin of facial diastereoselection. Evidence for negative role of antiperiplanar hyperconjugation effects in the transition state of carbene insertion

    • D. Kaneno, S. Tomoda
    Org. lett., 2003, 5, 2947-2949.
    DOI: https://doi.org/10.1021/ol035073c

  • Stereoelectronic and Conformational Effects on the Stereochemical Course of Reduction of Bicyclo[3.3.1]nonane 1,3-Diketones

    • E. Butkus, A. Stoncius, J. Malinauskiene, S. Tomoda, D. Kaneno
    Can. J. Chem., 2001, 79, 1598-1605.
    DOI: https://doi.org/10.1139/v01-131

  • π-Facial Diastereoselection of Hydride Reduction of 1,3-Diheteran-5-ones. Application of the Exterior Frontier Orbital Extension Model.

    • D. Kaneno, M. Iwaoka, J. Zhang, S. Tomoda
    Heteroatom Chem., 2001, 12, 358-368.
    DOI: https://doi.org/10.1002/hc.1055

  • Reversal of π-Facial Diastereoselection in the Hydride Reduction of Selenanones. Further Application of the Exterior Frontier Orbital Extension Model.

    • S. Tomoda, J. Zhang, D. Kaneno, M. Segi, A. Zhou
    Tetrahedron Lett., 2000, 41, 4597-4601.
    DOI: https://doi.org/10.1016/S0040-4039(00)00641-9

  • Origin of π-Facial Diastereoselection in Carbonyl addition. Application of the Exterior Frontier Orbital Extension Model to 1,3-Diheteran-5-ones (Heteroatom = O, S).

    • S. Tomoda, D. Kaneno, T. Senju
    Heterocycles, 2000, 52, 1435-1449.
    DOI: https://doi.org/10.3987/REV-99-SR7

  • Origin of π-facial stereoselection in nucleophilic additions to 1,3-diheteran-5-ones (heteroatom = O, S).Theoretical Evidence for the Importance of Ground-State Effects

    • S. Tomoda, D. Kaneno,T. Senju
    Chem. Lett., 1999, 1161-1162.
    DOI: https://doi.org/10.1246/cl.1999.1161

  • Stereochemical Determination of Acyclic Structures Based on Carbon-Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products

    • Matsumori, N.; Kaneno, D.; Murata, M.; Nakamura, H.; Tachibana, K.
    J. Org. Chem., 1999, 64, 866-876.
    DOI: https://doi.org/10.1021/jo981810k