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Results: 1-6 |
Results: 6

Authors: Kaneno, D Zhang, J Iwaoka, M Tomoda, S
Citation: D. Kaneno et al., pi-Facial diastereoselection of hydride reduction of 1,3-diheteran-5-ones:Application of the exterior frontier orbital extension model, HETEROAT CH, 12(5), 2001, pp. 358-368

Authors: Tomoda, S Kaneno, D
Citation: S. Tomoda et D. Kaneno, Prediction of facial diastereoselection with the exterior frontier orbitalextension model (EFOE model), J SYN ORG J, 59(3), 2001, pp. 219-231

Authors: Tomoda, S Kaneno, D Senju, T
Citation: S. Tomoda et al., Origin of pi-facial diastereoselection in carbonyl addition. Application of the exterior frontier orbital extension model to 1,3-diheteran-5-ones (heteroatom = O, S), HETEROCYCLE, 52(3), 2000, pp. 1435

Authors: Tomoda, S Zhang, J Kaneno, D Segi, M Zhou, AJ
Citation: S. Tomoda et al., Reversal of pi-facial diastereoselection in the hydride reduction of selenanones. Further application of the exterior frontier orbital extension model, TETRAHEDR L, 41(23), 2000, pp. 4597-4601

Authors: Tomoda, S Kaneno, D Senju, T
Citation: S. Tomoda et al., Origin of pi-facial diastereoselection in nucleophilic addition to 1,3-diheteran-5-ones (heteroatom = O, S). Theoretical evidence for the importance of ground-state effects, CHEM LETT, (11), 1999, pp. 1161-1162

Authors: Matsumori, N Kaneno, D Murata, M Nakamura, H Tachibana, K
Citation: N. Matsumori et al., Stereochemical determination of acyclic structures based on carbon-proton spin-coupling constants. A method of configuration analysis for natural products, J ORG CHEM, 64(3), 1999, pp. 866-876
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