BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 23225166)

  • 1. How the generalized anomeric effect influences the conformational preference.
    Wang C; Chen Z; Wu W; Mo Y
    Chemistry; 2013 Jan; 19(4):1436-44. PubMed ID: 23225166
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The generalized block-localized wavefunction method: a case study on the conformational preference and C-O rotational barrier of formic acid.
    Jia JF; Wu HS; Mo Y
    J Chem Phys; 2012 Apr; 136(14):144315. PubMed ID: 22502526
    [TBL] [Abstract][Full Text] [Related]  

  • 3. How solvent influences the anomeric effect: roles of hyperconjugative versus steric interactions on the conformational preference.
    Wang C; Ying F; Wu W; Mo Y
    J Org Chem; 2014 Feb; 79(4):1571-81. PubMed ID: 24456135
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Direct evaluation of the hyperconjugative interactions in 1,1,1-trihaloethane (CH3CX3, X = F, Cl, and Br).
    Chen Z; Corminboeuf C; Mo Y
    J Phys Chem A; 2014 Aug; 118(31):5743-7. PubMed ID: 24041308
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Computational evidence that hyperconjugative interactions are not responsible for the anomeric effect.
    Mo Y
    Nat Chem; 2010 Aug; 2(8):666-71. PubMed ID: 20651730
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exploring the Origin of the Generalized Anomeric Effects in the Acyclic Nonplanar Systems.
    Hasanzadeh N; Nori-Shargh D; Yahyaei H; Mousavi SN; Kamrava S
    J Phys Chem A; 2017 Jul; 121(29):5548-5560. PubMed ID: 28661674
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Electronic and steric substituent influences on the conformational equilibria of cyclohexyl esters: the anomeric effect is not anomalous!
    Kleinpeter E; Taddei F; Wacker P
    Chemistry; 2003 Mar; 9(6):1360-8. PubMed ID: 12645025
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Block-localized wavefunction (BLW) method at the density functional theory (DFT) level.
    Mo Y; Song L; Lin Y
    J Phys Chem A; 2007 Aug; 111(34):8291-301. PubMed ID: 17655207
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Atoms in molecules interpretation of the anomeric effect in the O--C--O unit.
    Vila A; Mosquera RA
    J Comput Chem; 2007 Jul; 28(9):1516-1530. PubMed ID: 17330885
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Steric strain versus hyperconjugative stabilization in ethane congeners.
    Song L; Lin Y; Wu W; Zhang Q; Mo Y
    J Phys Chem A; 2005 Mar; 109(10):2310-6. PubMed ID: 16839001
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interpretation of anomeric effect in the N-C-N unit with the quantum theory of atoms in molecules.
    Eskandari K; Vila A; Mosquera RA
    J Phys Chem A; 2007 Aug; 111(34):8491-9. PubMed ID: 17685599
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The anomeric effect on the basis of natural bond orbital analysis.
    Freitas MP
    Org Biomol Chem; 2013 May; 11(17):2885-90. PubMed ID: 23515623
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Anomeric effect in halogenated methanols: a quantum theory of atoms in molecules study.
    Ferro-Costas D; Vila A; Mosquera RA
    J Phys Chem A; 2013 Feb; 117(7):1641-50. PubMed ID: 23350752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dispersion-corrected energy decomposition analysis for intermolecular interactions based on the BLW and dDXDM methods.
    Steinmann SN; Corminboeuf C; Wu W; Mo Y
    J Phys Chem A; 2011 Jun; 115(21):5467-77. PubMed ID: 21557586
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Block-Localized Wavefunction (BLW) Based Two-State Approach for Charge Transfers between Phenyl Rings.
    Mo Y; Song L; Lin Y; Liu M; Cao Z; Wu W
    J Chem Theory Comput; 2012 Mar; 8(3):800-5. PubMed ID: 26593341
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Conformational preference of chlorothioformate species: molecular structure of ethyl chlorothioformate, ClC(O)SCH2CH3, in the solid phase and NBO analysis.
    Rodríguez Pirani L; Erben MF; Boese R; Pozzi CG; Fantoni AC; Della Védova CO
    Acta Crystallogr B; 2011 Aug; 67(Pt 4):350-6. PubMed ID: 21775813
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adjacent Lone Pair (ALP) Effect: A Computational Approach for Its Origin.
    Zhang H; Wu W; Ahmed BM; Mezei G; Mo Y
    Chemistry; 2016 May; 22(22):7415-21. PubMed ID: 27139318
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Substituent-dependent anomeric effects as a source of conformational preference in pyridinium methylides.
    Gupta N; Shah KK; Garg R
    J Org Chem; 2006 Feb; 71(4):1344-50. PubMed ID: 16468781
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Influence of the solvent on the charge distribution of anomeric compounds.
    Vila A; Estévez L; Mosquera RA
    J Phys Chem A; 2011 Mar; 115(10):1964-70. PubMed ID: 21322542
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Direct estimate of the strength of conjugation and hyperconjugation by the energy decomposition analysis method.
    Fernández I; Frenking G
    Chemistry; 2006 Apr; 12(13):3617-29. PubMed ID: 16502455
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.