Fulton, D.A., Elemento, E.M., Aime, S., Chaabane, L., Botta, M. and Parker, D. (2006) Glycoconjugates of Gadolinium Complexes for MRI Applications. Chemical Communications, 10, 1064-1066.
http://dx.doi.org/10.1039/b517997a

has been cited by the following article:

• TITLE: Branched Polyamines Functionalized with Proposed Reaction Pathways Based on 1H-NMR, Atomic Absorption and IR Spectroscopies

  AUTHORS: Vicente Cervantes-Mejía, Elizabeth Baca-Solis, Judith Caballero-Jiménez, Rosario Merino-García, Jesús Cruz-Gatica, Gabriela Moreno-Martínez, Yasmi Reyes-Ortega

  KEYWORDS: Branched Polyamines, Functionalization Reactions, IR, NMR, Atomic Absorption Spectroscopy

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.5 No.16, November 25, 2014

  ABSTRACT: Three novel branched polyamines N,N,N’,N’-tetrakis-[3((pyridine-2-methyl)-amine) propyl]-1,4- butanediamine (1), N,N,N’,N’-tetrakis-[N-((2-methylpyridine)ethyl)propanamide]ethylenediamine (2) and N,N,N’,N’-tetrakis-[3((2-hidroxibenziliden)-amine)propyl]-1,4-butanediamine (3), were synthesized starting from 2-pyridinecarboxaldeyde with DAB-Am-4 for 1, PAMAM G0 for 2 and from salicylaldehyde with DAB-Am-4 for 3. The pathway reactions have been proposed by 1H-NMR, IR and Atomic Absorption Spectroscopy. The optimal reaction time was set by IR spectroscopy following aldehyde peak modification. 1 and 2 were obtained as both hydrochlorides and as free amines and 3 only as free imine. These polyamines were characterized by UV-Vis, IR, 1H-NMR and 13C-NMR and Mass Spectrometry.