BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 34447565)

  • 1. An expanded halogen bonding scale using astatine.
    Liu L; Rahali S; Maurice R; Gomez Pech C; Montavon G; Le Questel JY; Graton J; Champion J; Galland N
    Chem Sci; 2021 Aug; 12(32):10855-10861. PubMed ID: 34447565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Towards a Stronger Halogen Bond Involving Astatine: Unexpected Adduct with Bu
    Liu L; Guo N; Champion J; Graton J; Montavon G; Galland N; Maurice R
    Chemistry; 2020 Mar; 26(17):3713-3717. PubMed ID: 31881101
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Experimental and computational evidence of halogen bonds involving astatine.
    Guo N; Maurice R; Teze D; Graton J; Champion J; Montavon G; Galland N
    Nat Chem; 2018 Apr; 10(4):428-434. PubMed ID: 29556053
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The diiodine basicity scale: toward a general halogen-bond basicity scale.
    Laurence C; Graton J; Berthelot M; El Ghomari MJ
    Chemistry; 2011 Sep; 17(37):10431-44. PubMed ID: 21834107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Astatine Facing Janus: Halogen Bonding vs. Charge-Shift Bonding.
    Sarr S; Pilmé J; Montavon G; Le Questel JY; Galland N
    Molecules; 2021 Jul; 26(15):. PubMed ID: 34361716
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complementary, Cooperative Ditopic Halogen Bonding and Electron Donor-Acceptor π-π Complexation in the Formation of Cocrystals.
    Speetzen ED; Nwachukwu CI; Bowling NP; Bosch E
    Molecules; 2022 Feb; 27(5):. PubMed ID: 35268629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bidentate Chiral Bis(imidazolium)-Based Halogen-Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis.
    Sutar RL; Engelage E; Stoll R; Huber SM
    Angew Chem Int Ed Engl; 2020 Apr; 59(17):6806-6810. PubMed ID: 32045504
    [TBL] [Abstract][Full Text] [Related]  

  • 8. On the Interplay between Charge-Shift Bonding and Halogen Bonding.
    Sarr S; Graton J; Montavon G; Pilmé J; Galland N
    Chemphyschem; 2020 Feb; 21(3):240-250. PubMed ID: 31793159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. N···I halogen bonding interactions: influence of Lewis bases on their strength and characters.
    Han N; Zeng Y; Sun C; Li X; Sun Z; Meng L
    J Phys Chem A; 2014 Aug; 118(34):7058-65. PubMed ID: 25102351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors.
    Yu S; Ward JS; Truong KN; Rissanen K
    Angew Chem Int Ed Engl; 2021 Sep; 60(38):20739-20743. PubMed ID: 34268851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is There a Single Ideal Parameter for Halogen-Bonding-Based Lewis Acidity?
    Engelage E; Reinhard D; Huber SM
    Chemistry; 2020 Mar; 26(17):3843-3861. PubMed ID: 31943430
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spin-orbit coupling as a probe to decipher halogen bonding.
    Graton J; Rahali S; Le Questel JY; Montavon G; Pilmé J; Galland N
    Phys Chem Chem Phys; 2018 Dec; 20(47):29616-29624. PubMed ID: 30318527
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Iodine(III)-Based Halogen Bond Donors: Properties and Applications.
    Robidas R; Reinhard DL; Legault CY; Huber SM
    Chem Rec; 2021 Aug; 21(8):1912-1927. PubMed ID: 34145711
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new type of halogen bond involving multivalent astatine: an ab initio study.
    Zhou F; Liu Y; Wang Z; Lu T; Yang Q; Liu Y; Zheng B
    Phys Chem Chem Phys; 2019 Jul; 21(28):15310-15318. PubMed ID: 31241070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An enthalpic scale of hydrogen-bond basicity. 4. Carbon pi bases, oxygen bases, and miscellaneous second-row, third-row, and fourth-row bases and a survey of the 4-fluorophenol affinity scale.
    Laurence C; Graton J; Berthelot M; Besseau F; Le Questel JY; Luçon M; Ouvrard C; Planchat A; Renault E
    J Org Chem; 2010 Jun; 75(12):4105-23. PubMed ID: 20491502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Halogen-bond geometry: a crystallographic database investigation of dihalogen complexes.
    Ouvrard C; Le Questel JY; Berthelot M; Laurence C
    Acta Crystallogr B; 2003 Aug; 59(Pt 4):512-26. PubMed ID: 12947237
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Catalytic activation
    Wang A; Kennepohl P
    Faraday Discuss; 2023 Aug; 244(0):241-251. PubMed ID: 37186101
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 2,2'-Bipyridine Derivatives as Halogen Bond Acceptors in Multicomponent Crystals.
    Kučas F; Posavec L; Nemec V; Bedeković N; Cinčić D
    Cryst Growth Des; 2023 Dec; 23(12):8482-8487. PubMed ID: 38089069
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Thermodynamics of halogen bonding in solution: substituent, structural, and solvent effects.
    Sarwar MG; Dragisic B; Salsberg LJ; Gouliaras C; Taylor MS
    J Am Chem Soc; 2010 Feb; 132(5):1646-53. PubMed ID: 20078063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Predictive Models for Halogen-bond Basicity of Binding Sites of Polyfunctional Molecules.
    Glavatskikh M; Madzhidov T; Solov'ev V; Marcou G; Horvath D; Graton J; Le Questel JY; Varnek A
    Mol Inform; 2016 Feb; 35(2):70-80. PubMed ID: 27491792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.