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Results:
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Results: 23
Authors:
Harada, T
Yoshida, H
Ohno, K
Matsuura, H
Zhang, J
Iwaoka, M
Tomoda, S
Citation: T. Harada et al., Implications of intramolecular OH center dot center dot center dot Se hydrogen bonding and CH center dot center dot center dot O interaction in the conformational stabilization of 2-(methylseleno)ethanol studied by vibrational spectroscopy and density functional theory, J PHYS CH A, 105(18), 2001, pp. 4517-4523
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:
Iwaoka, M
Takahashi, T
Tomoda, S
Citation: M. Iwaoka et al., Syntheses and structural characterization of water-soluble selenium reagents for the redox control of protein disulfide bonds, HETEROAT CH, 12(4), 2001, pp. 293-299
Authors:
Nakamura, T
Ishiko, O
Hirai, K
Sumi, T
Nakagawa, E
Nakai, Y
Tomoda, S
Ogita, S
Citation: T. Nakamura et al., Clinical evaluation of the Q-tip test in normal pregnant women, GYNECOL OBS, 51(2), 2001, pp. 92-95
Authors:
Iwaoka, M
Takemoto, S
Okada, M
Tomoda, S
Citation: M. Iwaoka et al., Statistical characterization of nonbonded S center dot center dot center dot O interactions in proteins, CHEM LETT, (2), 2001, pp. 132-133
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:
Iwaoka, M
Tomoda, S
Citation: M. Iwaoka et S. Tomoda, trans-3,4-Dihydroxy-1-selenolane oxide: A new reagent for rapid and quantitative formation of disulfide bonds in polypeptides, CHEM LETT, (12), 2000, pp. 1400-1401
Authors:
Iwaoka, M
Tomoda, S
Citation: M. Iwaoka et S. Tomoda, Nucleophilic selenium, T CURR CHEM, 208, 2000, pp. 55-80
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:
Iwaoka, M
Komatsu, H
Tomoda, S
Citation: M. Iwaoka et al., Structural characteristics of areneselenenyl bromide and areneselenenyl chloride stabilized by hypervalent coordination with a halide anion in the solid state, J ORGMET CH, 611(1-2), 2000, pp. 164-171
Authors:
Kuroda, S
Zuo, SL
Oda, M
Fukuta, A
Kajioka, T
Saito, T
Furuta, S
Tsukumo, H
Sano, K
Miyatake, R
Tomoda, S
Hayakawa, C
Nozawa, H
Citation: S. Kuroda et al., A convenient synthetic method for preparing 2,5-disubstituted 1,6-methano[10]annulenes from 1,6-diacetylcyclohepta-1,3,5-triene, B CHEM S J, 73(7), 2000, pp. 1659-1671
Authors:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Quantitative evaluation of steric effects for pi-facial stereoselection: pi-plane-divided accessible space, CHEM COMMUN, (7), 1999, pp. 621-622
Authors:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Natural bond orbital analysis of hyperconjugative stabilization effects inthe transition states of cyclohexanone reduction with LiAlH4, CHEM COMMUN, (5), 1999, pp. 423-424
Authors:
Komatsu, H
Iwaoka, M
Tomoda, S
Citation: H. Komatsu et al., Intramolecular non-bonded interaction between selenium and oxygen as revealed by O-17 and Se-77 NMR spectroscopy and natural bond orbital analysis, CHEM COMMUN, (2), 1999, pp. 205-206
Authors:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Origin of pi-facial diastereoselection in hydride reduction of piperidones. The importance of ground-state effects, CHEM LETT, (7), 1999, pp. 625-626
Authors:
Ikeno, T
Harada, J
Tomoda, S
Citation: T. Ikeno et al., Structure and natural bond orbital analysis of oxiranes substituted with agroup 14 element. A comment of SN2 regioselectivity, CHEM LETT, (5), 1999, pp. 409-410
Authors:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Origin of pi-facial stereoselectivity in nucleophilic addition. Application of the exterior frontier orbital extension model to substituted bicyclo[2.2.1]heptan-7-ones, CHEM LETT, (4), 1999, pp. 353-354
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:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Origin of pi-facial stereoselection in nucleophilic additions of adamantanones. A new interpretation based on the exterior frontier orbital extensionmodel, TETRAHEDRON, 55(17), 1999, pp. 5303-5318
Authors:
Tomoda, S
Senju, T
Citation: S. Tomoda et T. Senju, Origin of pi-facial stereoselectivity of nucleophilic addition to carbonylcompounds. Application of the exterior frontier orbital extension model tocyclohexanones with polar substituent, TETRAHEDRON, 55(13), 1999, pp. 3871-3882
Authors:
Tomoda, S
Senju, T
Kawamura, M
Ikeda, T
Citation: S. Tomoda et al., Origin of pi-facial stereoselectivity in nucleophilic additions. Application of the exterior frontier orbital extension model to imines and iminium ions, J ORG CHEM, 64(15), 1999, pp. 5396-5400
Authors:
Tomoda, S
Citation: S. Tomoda, The exterior frontier orbital extension model, CHEM REV, 99(5), 1999, pp. 1243-1263
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