BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

308 related articles for article (PubMed ID: 23848404)

  • 1. Chiral recognition of amino acid enantiomers by a crown ether: chiroptical IR-VCD response and computational study.
    Avilés-Moreno JR; Quesada-Moreno MM; López-González JJ; Martínez-Haya B
    J Phys Chem B; 2013 Aug; 117(32):9362-70. PubMed ID: 23848404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural scaffold of 18-crown-6 tetracarboxylic acid for optical resolution of chiral amino acid: X-ray crystal analyses and energy calculations of complexes of D- and L-isomers of tyrosine, isoleucine, methionine and phenylglycine.
    Nagata H; Nishi H; Kamigauchi M; Ishida T
    Org Biomol Chem; 2004 Dec; 2(23):3470-5. PubMed ID: 15565239
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multipodal coordination of a tetracarboxylic crown ether with NH4(+): a vibrational spectroscopy and computational study.
    Hurtado P; Gámez F; Hamad S; Martínez-Haya B; Steill JD; Oomens J
    J Chem Phys; 2012 Mar; 136(11):114301. PubMed ID: 22443758
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Guest-dependent conformation of 18-crown-6 tetracarboxylic acid: relation to chiral separation of racemic amino acids.
    Nagata H; Nishi H; Kamigauchi M; Ishida T
    Chirality; 2008 Jul; 20(7):820-7. PubMed ID: 18306294
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Noncovalent interactions between ([18]crown-6)-tetracarboxylic acid and amino acids: electrospray-ionization mass spectrometry investigation of the chiral-recognition processes.
    Gerbaux P; De Winter J; Cornil D; Ravicini K; Pesesse G; Cornil J; Flammang R
    Chemistry; 2008; 14(35):11039-49. PubMed ID: 18956399
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chiral NMR discrimination of piperidines and piperazines using (18-crown-6)-2,3,11,12-tetracarboxylic acid.
    Lovely AE; Wenzel TJ
    J Org Chem; 2006 Nov; 71(24):9178-82. PubMed ID: 17109544
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Simulations of solid-state vibrational circular dichroism spectroscopy of (S)-alternarlactam by using fragmentation quantum chemical calculations.
    Jiang N; Tan RX; Ma J
    J Phys Chem B; 2011 Mar; 115(12):2801-13. PubMed ID: 21391541
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absolute configuration and predominant conformations of a chiral crown ether-based colorimetric sensor: a vibrational circular dichroism spectroscopy and DFT study of chiral recognition.
    Merten C; Hyun MH; Xu Y
    Chirality; 2013 May; 25(5):294-300. PubMed ID: 23620265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural scaffold of 18-crown-6 tetracarboxylic Acid for optical resolution of chiral amino acid: x-ray crystal analyses of complexes of D- and L-isomers of serine and glutamic acid.
    Nagata H; Nishi H; Kamigauchi M; Ishida T
    Chem Pharm Bull (Tokyo); 2006 Apr; 54(4):452-7. PubMed ID: 16595944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectroscopy, NMR and DFT studies on molecular recognition of crown ether bridged chiral heterotrinuclear salen Zn(II) complex.
    Gao F; Ruan WJ; Chen JM; Zhang YH; Zhu ZA
    Spectrochim Acta A Mol Biomol Spectrosc; 2005 Dec; 62(4-5):886-95. PubMed ID: 15897004
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Infrared spectroscopy of ionophore-model systems: hydrated alkali metal ion 18-crown-6 ether complexes.
    Rodriguez JD; Vaden TD; Lisy JM
    J Am Chem Soc; 2009 Dec; 131(47):17277-85. PubMed ID: 19899741
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Guanidinium/ammonium competition and proton transfer in the interaction of the amino acid arginine with the tetracarboxylic 18-crown-6 ionophore.
    Avilés-Moreno JR; Berden G; Oomens J; Martínez-Haya B
    Phys Chem Chem Phys; 2018 Feb; 20(6):4067-4073. PubMed ID: 29354835
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Vibrational circular dichroism and IR absorption spectra of amino acids: a density functional study.
    Ji Z; Santamaria R; Garzón IL
    J Phys Chem A; 2010 Mar; 114(10):3591-601. PubMed ID: 20155958
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of chiral separations of aminophosphonic acids and their aminocarboxylic acid analogs using a crown ether column.
    Barnhart WW; Xia X; Jensen R; Gahm KH
    Chirality; 2013 Jul; 25(7):369-78. PubMed ID: 23703726
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Enantiomeric discrimination of isoxazoline fused β-amino acid derivatives using (18-crown-6)-2,3,11,12-tetracarboxylic acid as a chiral NMR solvating agent.
    Howard JA; Nonn M; Fulop F; Wenzel TJ
    Chirality; 2013 Jan; 25(1):48-53. PubMed ID: 23161804
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Enantiomeric separation of chiral dipeptides by CE-ESI-MS employing a partial filling technique with chiral crown ether.
    Xia S; Zhang L; Lu M; Qiu B; Chi Y; Chen G
    Electrophoresis; 2009 Aug; 30(16):2837-44. PubMed ID: 19655329
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Competitive binding of a Tris run buffer with chiral crown ether in chiral capillary electrophoresis.
    Cho SI; Jung H; Chung DS
    Electrophoresis; 2000 Nov; 21(17):3618-24. PubMed ID: 11271479
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Conformations of serine in aqueous solutions as revealed by vibrational circular dichroism.
    Zhu P; Yang G; Poopari MR; Bie Z; Xu Y
    Chemphyschem; 2012 Apr; 13(5):1272-81. PubMed ID: 22334359
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Preparation of a new crown ether-based chiral stationary phase containing thioester linkage for the liquid chromatographic separation of enantiomers.
    Cho HS; Choi HJ; Hyun MH
    J Chromatogr A; 2009 Oct; 1216(44):7446-9. PubMed ID: 19406408
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stereoisomeric separation of pharmaceutical compounds using CE with a chiral crown ether.
    Zhou L; Lin Z; Reamer RA; Mao B; Ge Z
    Electrophoresis; 2007 Aug; 28(15):2658-66. PubMed ID: 17657760
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.