Duane Choquesillo-Lazarte-rekin lankidetzan egindako argitalpenak (10)

2023

  1. H(N3)dap (Hdap = 2,6-Diaminopurine) Recognition by Cu2(EGTA): Structure, Physical Properties, and Density Functional Theory Calculations of [Cu4(μ-EGTA)2(μ-H(N3)dap)2(H2O)2]·7H2O

    Molecules, Vol. 28, Núm. 17

  2. Supramolecular Nature of Multicomponent Crystals Formed from 2,2′-Thiodiacetic Acid with 2,6-Diaminopurine or N9-(2-Hydroxyethyl)adenine

    International Journal of Molecular Sciences, Vol. 24, Núm. 24

2021

  1. Dicopper(Ii)-edta chelate as a bicephalic receptor model for a synthetic adenine nucleoside

    Pharmaceuticals, Vol. 14, Núm. 5

2020

  1. Molecular and supramolecular recognition patterns in ternary copper(II) or zinc(II) complexes with selected rigid-planar chelators and a synthetic adenine-nucleoside

    Journal of Inorganic Biochemistry, Vol. 203

2018

  1. Copper(II) polyamine chelates as efficient receptors for acyclovir: syntheses, crystal structures and dft study

    Polyhedron, Vol. 145, pp. 218-226

2016

  1. Metal binding pattern of acyclovir in ternary copper(II) complexes having an S-thioether or S-disulfide NO2S-tripodal tetradentate chelator

    Inorganica Chimica Acta, Vol. 452, pp. 258-267

2015

  1. Metal complexes with N-(trifluoromethylbenzyl)iminodiacetate chelators (x-3F ligands). Part I. Copper(II) chelates of p-3F, m-3F, and o-3F with or without imidazole-like ligands

    Journal of Coordination Chemistry, Vol. 68, Núm. 16, pp. 2739-2759

  2. Molecular recognition between adenine or 2,6-diaminopurine and copper(II) chelates with N,O2,S-tripodal tetradentate chelators having thioether or disulfide donor groups

    Journal of Inorganic Biochemistry, Vol. 151, pp. 75-86

2014

  1. Stereospecific alkylation of substituted adenines by the Mitsunobu coupling reaction under microwave-assisted conditions

    RSC Advances, Vol. 4, Núm. 43, pp. 22425-22433

2013

  1. Enantiospecific synthesis of heterocycles linked to purines: Different apoptosis modulation of enantiomers in breast cancer cells

    Current Medicinal Chemistry, Vol. 20, Núm. 38, pp. 4924-4934