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Personal docente e investigador

Rodríguez Solla, Humberto

Categoría:
Profesor Titular
Teléfono:
985103499
Correo:
hrsolla@uniovi.es
Despacho:
320

Áreas de interés:

  • Síntesis Organometálica

Publicaciones:

  • Synthesis and Sythetic Applications of Samarium Enolates of Unmasked Amides: Efficient Synthesis of 3-Amino-2- Chloroamides. Synlett 2010, 2119-2121
  • Highly Enantioselective Proline-Catalysed Direct Aldol Reaction of Chloroacetone and Aromatic Aldehydes.Chem. Eur. J. 2012, 18, 5188- 5190
  • Asymmetric Construction of Quaternary Sterocenters: Synthesis of Enantiopure Amino Acid-Based Tricyclic a,b-Enones through an ipso-Friedel-Crafts/Michael Addition Cascade. Adv. Synth. Catal. 2012, 354, 295- 300
  • TBD/Al2O3: A Novel Catalytic System for Dynamic Intermolecular Aldol Reactions that Exhibit Complex System Behaviour. Org. Biomol. Chem. 2012, 10, 1976- 1981
  • The use of samarium or sodium iodides as a novel alternative for the aza-Henry reaction. Tetrahedron 2012, 68, 1736-1744
  • Chromium-Mediated Stereoselective Synthesis of Carbohydrate-Derived (E)-α,β-Unsaturated Esters or Amides. J. Org. Chem. 2011, 76, 5461-5465
  • Direct Aldol Reactions Catalyzed by a Heterogeneous Guanidinium Salt/Proline System under Solvent-Free Conditions. Org. Lett. 2011, 13, 3032-3035
  • An Efficient Catalytic-Chromium Mediated Iodocyclopropanation Reaction: Stereoselective Synthesis of Iodocyclopropanecarboxamides. Adv. Synth. Catal. 2011, 352, 49-52
  • A convenient synthesis of (E)-a,b-unsaturated esters with total stereoselectivity promoted by catalytic samarium diiodide. Synlett 2011, 2, 262-264.
  • Stereospecific and hghly stereoselective cyclopropanation reactions promoted by samarium. Chem. Soc. Rev. 2010, 39, 4103-4113