Almodóvar Fajardo Iriux

Email: 
iriux.almodovar@usach.cl
Teléfono: 
27 181 161
Sitio web: 
Sitio web

Abstract

Developing of green synthetic strategies to obtain compounds with interesting pharmacological properties.

Jerarquía: 
Asistente
Línea de investigación: 
Síntesis Orgánica - Mecanismos de reacción.
Grados académicos /educación: 
Químico, Universidad de La Habana, 1996
Doctor en Química, Universidad de Chile, 2006.
Publicaciones: 
  • C. Aliaga, I. Almodovar and M. C. Rezende, A single theoretical descriptor for the bond-dissociation energy of substituted phenols, J. Mol. Model., 21 (2015), 2572. Impact Factor=1.867I.
  • M. C. Rezende, I. Ponce, R. Oñate, I. Almodovar, C. Aliaga. Change of mechanism with a change of substituents for a Zincke reaction. Tetrahedron Letters 55 (2014) 3097. Impact Factor= 2.397.
  • P. Abarca, P. Silva, I. Almodovar, M. C. Rezende* Preparation and properties of perichromic dye: an undergraduate laboratory, Quim. Nova, 37(4) (2014) 745. Impact Factor =0.737.
  • I. Almodovar*, T. Delgado-Castro, G. Zapata-Torres, M. C Rezende, R. Araya-Maturana, Factors affecting the competitive reduction of 8,8-dimethylnaphthalene-1,4,5(8H)-trione in a Diels-Alder cycloaddition with hydroxysulfinyldienes. J.Iran.Chem.Soc., (2014), Volume 11, Issue 4, 1021-1026 . Impact Factor= 1.467.
  • I. Almodovar*, W. Cardona, T. Delgado-Castro, G. Zapata-Torres, M. C. Rezende, R. Araya-Maturana, M. C. Maestro, J. L. García Ruano, Remote regio- and stereocontrol by the sulfinyl group. Diels-Alder reaction of sulfinyl dienols and 8,8-dimethylnaphthalene-1,4,5(8H)-trione. Tetrahedron: Asymmetry, 24 (2013) 56. Impact Factor= 2.652.
  • M. A. Juricic*, P. A. Berríos-Cárcamo, M. L. Acevedo, Y. Israel, I. Almodovar, B. K. Cassels, Salsolinol and isosalsolinol: condensation products of acetaldehyde and dopamine.Separation of their enantiomers in the presence of a large excess of dopamine. Journal of pharmaceutical and biomedical analysis, 63 (2012) 170. Impact Factor=2.723.
  • M. C. Rezende*, I. Almodovar, Substituent electrophilicities in the NMR spectra of barbituric Derivatives, Magnetic Resonance in Chemistry, 50 (2012) 266. IF= 1,247.
  • H. Pessoa-Mahana*, I. M. Cuevas, D. C. Pessoa-Mahana, R. Araya-Maturana, I. Almodovar and C. A. Saitz-Barrá, Synthesis of 1-Benzyl-3-[4-(Aryl-1-Piperazinyl) Carbonyl]-1h-Indoles: Novel Ligands With Potential D4 Dopaminergic Activity. Journal of Chilean Chemical Society, 56, 4 (2011) 866. Impact Factor= 0.448.
  • I. Almodovar*, O. Ramírez-Rodríguez, A. Barriga, M. C. Rezende, R. Araya-Maturana, Electrospray ionization mass spectrometric fragmentation of hydroquinone derivatives. Rapid Commun. Mass Spectrom. 25 (2) (2011) 370. Impact Factor=2.846.
Proyectos: 
Fondecyt
 
Nº 11121270 (Iniciación).  Investigadora Principal. 2012 - 2015.
 
Nº 3100059 (Postdoctorado). Investigadora Principal. 2009 - 2012.