These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 21067236)

  • 21. Predicting reduction potentials of 1,3,6-triphenyl fulvenes using molecular electrostatic potential analysis of substituent effects.
    Anjali BA; Suresh CH
    J Comput Chem; 2018 Jun; 39(15):881-888. PubMed ID: 29322538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Remote substituent effects on N-X (X = H, F, Cl, CH3, Li) bond dissociation energies in para-substituted anilines.
    Song KS; Liu L; Guo QX
    J Org Chem; 2003 Jan; 68(2):262-6. PubMed ID: 12530847
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evidence of substituent-induced electronic interplay. Effect of the remote aromatic ring substituent of phenyl benzoates on the sensitivity of the carbonyl unit to electronic effects of phenyl or benzoyl ring substituents.
    Neuvonen H; Neuvonen K; Pasanen P
    J Org Chem; 2004 May; 69(11):3794-800. PubMed ID: 15153011
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Does tetrahydrofuran ring open upon ionization and dissociation? A TPES and TPEPICO investigation.
    Mayer PM; Guest MF; Cooper L; Shpinkova LG; Rennie EE; Holland DM; Shaw DA
    J Phys Chem A; 2009 Oct; 113(41):10923-32. PubMed ID: 19775111
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Structures, electron affinities, and harmonic vibrational frequencies of C6H5X/C6H5X- (X = N, S, NH, PH, CH2, and SiH2).
    Xu W; Gao A
    J Phys Chem A; 2006 Jan; 110(3):997-1004. PubMed ID: 16420000
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The peculiar trend of cyclic perfluoroalkane electron affinities with increasing ring size.
    Paul A; Wannere CS; Kasalova V; Schleyer Pv; Schaefer HF
    J Am Chem Soc; 2005 Nov; 127(44):15457-69. PubMed ID: 16262410
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Design of TTF-based phosphazenes combining a good electron-donor capacity and possible inclusion adduct formation.
    Gahungu G; Zhang B; Zhang J
    J Phys Chem B; 2006 Aug; 110(34):16852-9. PubMed ID: 16927972
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Theoretical study on photophysical properties of multifunctional electroluminescent molecules with different pi-conjugated bridges.
    Zou LY; Ren AM; Feng JK; Liu YL; Ran XQ; Sun CC
    J Phys Chem A; 2008 Nov; 112(47):12172-8. PubMed ID: 18959398
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Theoretical investigation of optical and electronic property modulations of pi-conjugated polymers based on the electron-rich 3,6-dimethoxy-fluorene unit.
    Yang L; Ren AM; Feng JK; Wang JF
    J Org Chem; 2005 Apr; 70(8):3009-20. PubMed ID: 15822959
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Accurate prediction for electron affinities of the radicals derived from the halide benzene.
    Xu W; Gao A
    J Chem Phys; 2005 Aug; 123(8):084320. PubMed ID: 16164304
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Silicon monohydride clusters Si(n)H (n = 4-10) and their anions: structures, thermochemistry, and electron affinities.
    Yang J; Bai X; Li C; Xu W
    J Phys Chem A; 2005 Jun; 109(25):5717-23. PubMed ID: 16833904
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Exploiting the Aromatic Chameleon Character of Fulvenes for Computational Design of Baird-Aromatic Triplet Ground State Compounds.
    Yadav S; El Bakouri O; Jorner K; Tong H; Dahlstrand C; Solà M; Ottosson H
    Chem Asian J; 2019 May; 14(10):1870-1878. PubMed ID: 30659757
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel fused D-A dyad and A-D-A triad incorporating tetrathiafulvalene and p-benzoquinone.
    Dumur F; Gautier N; Gallego-Planas N; Sahin Y; Levillain E; Mercier N; Hudhomme P; Masino M; Girlando A; Lloveras V; Vidal-Gancedo J; Veciana J; Rovira C
    J Org Chem; 2004 Mar; 69(6):2164-77. PubMed ID: 15058966
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Calculation of electron affinities of polycyclic aromatic hydrocarbons and solvation energies of their radical anion.
    Betowski LD; Enlow M; Riddick L; Aue DH
    J Phys Chem A; 2006 Nov; 110(47):12927-46. PubMed ID: 17125310
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Theoretical study of the substituent effects on the S-H bond dissociation energy and ionization energy of 3-pyridinethiol: Prediction of novel antioxidant.
    Nam PC; Nguyen MT; Chandra AK
    J Phys Chem A; 2006 Sep; 110(37):10904-11. PubMed ID: 16970388
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Stability and reactivity of grafted Cr(CO)3 species on MOF linkers: a computational study.
    Vitillo JG; Groppo E; Bordiga S; Chavan S; Ricchiardi G; Zecchina A
    Inorg Chem; 2009 Jun; 48(12):5439-48. PubMed ID: 19499958
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Theoretical studies on four-membered ring compounds with NF2, ONO2, N3, and NO2 groups.
    Fan XW; Ju XH
    J Comput Chem; 2008 Mar; 29(4):505-13. PubMed ID: 17663437
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Determination of the electron affinities of alpha- and beta-naphthyl radicals using the kinetic method with full entropy analysis. The C-H bond dissociation energies of naphthalene.
    Lardin HA; Squires RR; Wenthold PG
    J Mass Spectrom; 2001 Jun; 36(6):607-15. PubMed ID: 11433533
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Predicting hydrogen-bond strengths from acid-base molecular properties. The pK(a) slide rule: toward the solution of a long-lasting problem.
    Gilli P; Pretto L; Bertolasi V; Gilli G
    Acc Chem Res; 2009 Jan; 42(1):33-44. PubMed ID: 18921985
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Substituent Effects on the Absorption and Fluorescence Properties of Anthracene.
    Abou-Hatab S; Spata VA; Matsika S
    J Phys Chem A; 2017 Feb; 121(6):1213-1222. PubMed ID: 28103041
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.