BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

390 related articles for article (PubMed ID: 24598905)

  • 1. Exploring the structure-aromaticity relationship in Hückel and Möbius N-fused pentaphyrins using DFT.
    Alonso M; Geerlings P; De Proft F
    Phys Chem Chem Phys; 2014 Jul; 16(28):14396-407. PubMed ID: 24598905
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Viability of Möbius topologies in [26]- and [28]hexaphyrins.
    Alonso M; Geerlings P; de Proft F
    Chemistry; 2012 Aug; 18(35):10916-28. PubMed ID: 22806882
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Conformational control in [22]- and [24]pentaphyrins(1.1.1.1.1) by meso substituents and their N-fusion reaction.
    Alonso M; Geerlings P; De Proft F
    J Org Chem; 2013 May; 78(9):4419-31. PubMed ID: 23551193
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Understanding the molecular switching properties of octaphyrins.
    Woller T; Contreras-García J; Geerlings P; De Proft F; Alonso M
    Phys Chem Chem Phys; 2016 Apr; 18(17):11885-900. PubMed ID: 26924378
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Switching between Hückel and Möbius aromaticity: a density functional theory and information-theoretic approach study.
    Yu D; Rong C; Lu T; Geerlings P; De Proft F; Alonso M; Liu S
    Phys Chem Chem Phys; 2020 Feb; 22(8):4715-4730. PubMed ID: 32057037
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Macrocyclic aromaticity in Hückel and Möbius conformers of porphyrinoids.
    Aihara J; Horibe H
    Org Biomol Chem; 2009 May; 7(9):1939-43. PubMed ID: 19590791
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Topology switching in [32]heptaphyrins controlled by solvent, protonation, and meso substituents.
    Alonso M; Geerlings P; De Proft F
    Chemistry; 2013 Jan; 19(5):1617-28. PubMed ID: 23255381
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Temperature-dependent conformational change of meso-hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into Möbius structures.
    Kim KS; Yoon ZS; Ricks AB; Shin JY; Mori S; Sankar J; Saito S; Jung YM; Wasielewski MR; Osuka A; Kim D
    J Phys Chem A; 2009 Apr; 113(16):4498-506. PubMed ID: 19265390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Conductance Switching in Expanded Porphyrins through Aromaticity and Topology Changes.
    Stuyver T; Perrin M; Geerlings P; De Proft F; Alonso M
    J Am Chem Soc; 2018 Jan; 140(4):1313-1326. PubMed ID: 29291371
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unveiling Möbius/Hückel Topology and Aromaticity in A Core-Expanded [10]Annulene at Different Oxidation States.
    Wu S; Han Y; Ni Y; Hou X; Wei H; Li Z; Wu J
    Angew Chem Int Ed Engl; 2024 Mar; 63(11):e202320144. PubMed ID: 38243691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hückel and Möbius expanded para-benziporphyrins: synthesis and aromaticity switching.
    Szyszko B; Sprutta N; Chwalisz P; Stępień M; Latos-Grażyński L
    Chemistry; 2014 Feb; 20(7):1985-97. PubMed ID: 24431244
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Stable Non-fused [22]Pentaphyrins and A Fused [24]Pentaphyrin Displaying Crystal Polymorphism between Hückel and Möbius Structures.
    Yoneda T; Hoshino T; Neya S
    Chem Asian J; 2017 Feb; 12(4):405-409. PubMed ID: 28028937
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effect of the meso-substituent in the Hückel-to-Möbius topological switches.
    Marcos E; Anglada JM; Torrent-Sucarrat M
    J Org Chem; 2014 Jun; 79(11):5036-46. PubMed ID: 24816245
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ESI-MS/MS of expanded porphyrins: a look into their structure and aromaticity.
    Ramos CI; Figueira F; Polêto MD; Amado FM; Verli H; Tomé JP; Neves MG
    J Mass Spectrom; 2016 May; 51(5):342-9. PubMed ID: 27194518
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1).
    Sankar J; Mori S; Saito S; Rath H; Suzuki M; Inokuma Y; Shinokubo H; Kim KS; Yoon ZS; Shin JY; Lim JM; Matsuzaki Y; Matsushita O; Muranaka A; Kobayashi N; Kim D; Osuka A
    J Am Chem Soc; 2008 Oct; 130(41):13568-79. PubMed ID: 18808116
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Protonated [4n]pi and [4n+2]pi octaphyrins choose their Möbius/Hückel aromatic topology.
    Lim JM; Shin JY; Tanaka Y; Saito S; Osuka A; Kim D
    J Am Chem Soc; 2010 Mar; 132(9):3105-14. PubMed ID: 20148589
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three-level topology switching in a molecular Möbius band.
    Stepień M; Szyszko B; Latos-Grazyński L
    J Am Chem Soc; 2010 Mar; 132(9):3140-52. PubMed ID: 20155939
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pd(II) complexes of [44]- and [46]decaphyrins: the largest Hückel aromatic and antiaromatic, and Möbius aromatic macrocycles.
    Yoneda T; Sung YM; Lim JM; Kim D; Osuka A
    Angew Chem Int Ed Engl; 2014 Nov; 53(48):13169-73. PubMed ID: 25258332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
    Szczepanik DW; Solà M
    ChemistryOpen; 2019 Feb; 8(2):219-227. PubMed ID: 30828509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation of the nonlinear optical properties for an expanded porphyrin Hückel-Möbius aromaticity switch.
    Torrent-Sucarrat M; Anglada JM; Luis JM
    J Chem Phys; 2012 Nov; 137(18):184306. PubMed ID: 23163370
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.