Publications en collaboration avec des chercheurs de Instituto de Química Orgánica General (11)

2016

  1. Click chemistry to fluorescent hyperbranched polymeric sensors. 2. Synthesis, spectroscopic and cation-sensing properties of new green fluorescent 1,8-naphthalimides

    European Polymer Journal, Vol. 74, pp. 241-255

2014

  1. Click chemistry to fluorescent hyperbranched polymers. 1 - Synthesis, characterization and spectroscopic properties

    European Polymer Journal, Vol. 59, pp. 290-301

2012

  1. Catalyst development for organocatalytic hydrosilylation of aromatic ketones and ketimines

    Organic and Biomolecular Chemistry, Vol. 10, Núm. 25, pp. 4864-4877

2011

  1. A new family of "clicked" estradiol-based low-molecular-weight gelators having highly symmetry-dependent gelation ability

    Chemical Communications, Vol. 47, Núm. 37, pp. 10281-10283

  2. C-Branched chiral (racemic) macrocyclic amino acids: Structure of their Ni(ii), Zn(ii) and Cu(ii) complexes

    Dalton Transactions, Vol. 40, Núm. 36, pp. 9145-9153

2010

  1. Two versatile and parallel approaches to highly symmetrical open and closed natural product-based structures

    Chemistry - A European Journal, Vol. 16, Núm. 12, pp. 3798-3814

2009

  1. A copper-catalyzed azide-alkyne cycloaddition approach to the synthesis of bimetallic chromium(o) (fischer) carbene complexes

    Organometallics, Vol. 28, Núm. 4, pp. 956-959

  2. The assembly of macrocyclic bis- And tetra-β-lactams with embedded platinum or palladium square-planar centers

    Chemistry - A European Journal, Vol. 15, Núm. 28, pp. 6940-6952

2008

  1. A straightforward synthesis of tetrameric estrone-based macrocycles

    Organic Letters, Vol. 10, Núm. 16, pp. 3555-3558

  2. On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosilanes catalyzed by QUINOX, a chiral isoquinoline N-oxide

    Journal of the American Chemical Society, Vol. 130, Núm. 15, pp. 5341-5348

2005

  1. Understanding of the mode of action of FeIII-EDDHA as iron chlorosis corrector based on its photochemical and redox behavior

    Chemistry - A European Journal, Vol. 11, Núm. 20, pp. 5997-6005