Publications (-2010)
Reviews
- Prediction of facial diastereoselection with the exterior frontier orbital extension model (EFOE model)
Tomoda, S.; Kaneno, D.
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 2001, 59, 219-231.
DOI: https://doi.org/10.5059/yukigoseikyokaishi.59.219
Publications
- Intramolecular titanium-promoted deoxygenative cyclization to 9-substituted-1,2,3,4-tetrahydrofluorene skeleton
- Theoretical Study on the Mechanism and Diastereoselectivity of NaBH4 Reduction
- The Danishefsky Pyranone Puzzle. An Explanation based on the Exterior Frontier Orbital Extension Model
- The Importance of Lone Pair Delocalizations: Theoretical Investigations on the Stability of cis and trans Isomers in 1,2-Halodiazenes
- Solvent effects on the diastereoselection in LiAlH4 reduction of α-substituted ketones
- The Origin of Cis-Effect in 1,2-Dihaloethenes: The Quantitative Comparison of Electron Delocalizations and Steric Exchange Repulsions
- The Importance of Lone Pair Electron Delocalization in the cis-trans Isomers of 1,2-Dibromoethenes
- Origin of facial diastereoselection in 2-adamantyl cations. Theoretical evidence against the Felkin-Anh and the Cieplak models
- Origin of diastereoselection in the hydrosilylation of chiral N-acyliminium intermediates derived from pyroglutamic acid
- Origin of facial diastereoselection. Evidence for negative role of antiperiplanar hyperconjugation effects in the transition state of carbene insertion
- Stereoelectronic and Conformational Effects on the Stereochemical Course of Reduction of Bicyclo[3.3.1]nonane 1,3-Diketones
- π-Facial Diastereoselection of Hydride Reduction of 1,3-Diheteran-5-ones. Application of the Exterior Frontier Orbital Extension Model.
- Reversal of π-Facial Diastereoselection in the Hydride Reduction of Selenanones. Further Application of the Exterior Frontier Orbital Extension Model.
- 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).
- 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
- Stereochemical Determination of Acyclic Structures Based on Carbon-Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products
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
Suzuki, Y.; Kaneno, D.; Tomoda.
J. Phys. Chem. A., 2009, 113, 2578-2583.
DOI: https://doi.org/10.1021/jp809966u
Kaneno, D.; Tomoda, S.
Tetrahedron Lett., 2009, 50, 329-332.
DOI: https://doi.org/10.1016/j.tetlet.2008.11.004
Yamamoto, T.; Kaneno, D.; Tomoda, S.
J. Org. Chem., 2008, 73, 15429-5435.
DOI: https://doi.org/10.1021/jo8006896
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
Yamamoto, T.; Kaneno, D.; Tomoda, S.
Bull. Chem. Soc. Jpn., 2008, 81, 1415-1422.
DOI: https://doi.org/10.1246/bcsj.81.1415
Yamamoto, T.; Kaneno, D.; Tomoda, S.
Chem. lett., 2005, 34, 1190-1191.
DOI: https://doi.org/10.1246/cl.2005.1190
D. Kaneno, S. Tomoda
Tetrahedron lett., 2004, 45, 4559-4562.
DOI: https://doi.org/10.1016/j.tetlet.2004.04.036
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
D. Kaneno, S. Tomoda
Org. lett., 2003, 5, 2947-2949.
DOI: https://doi.org/10.1021/ol035073c
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
D. Kaneno, M. Iwaoka, J. Zhang, S. Tomoda
Heteroatom Chem., 2001, 12, 358-368.
DOI: https://doi.org/10.1002/hc.1055
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
S. Tomoda, D. Kaneno, T. Senju
Heterocycles, 2000, 52, 1435-1449.
DOI: https://doi.org/10.3987/REV-99-SR7
S. Tomoda, D. Kaneno,T. Senju
Chem. Lett., 1999, 1161-1162.
DOI: https://doi.org/10.1246/cl.1999.1161
Matsumori, N.; Kaneno, D.; Murata, M.; Nakamura, H.; Tachibana, K.
J. Org. Chem., 1999, 64, 866-876.
DOI: https://doi.org/10.1021/jo981810k