Research group on asymmetric catalysis with metal complexes and organocatalysts - AsymCat

Reference of the Group:

GIUV2013-125

 
Description of research activity:
Chirality is a property related to the three-dimensional shape of molecules. Chiral molecules can exist in two forms (enantiomers) that are mirror images of each other. This subtle difference has tremendously important implications in chemistry, as two enantiomers can exhibit completely different or even opposite biological or pharmacological properties. Similarly, the mechanical, magnetic or electrical properties of many materials can vary completely depending on whether they are made up of a single enantiomer or mixtures of enantiomers. As a consequence of all this, there is a real need at both laboratory and industrial level for synthetic procedures that allow chiral compounds to be obtained selectively in a defined enantiomeric form. Among the different methodologies available for this purpose, those using chiral catalysts are the most suitable, as they allow minimising the consumption of chiral starting materials and reducing waste production, contributing to more efficient, more economical and more environmentally friendly chemical processes. In this context, the asymmetric catalysis group investigates the development of new chiral catalysts based on both metal complexes and...Chirality is a property related to the three-dimensional shape of molecules. Chiral molecules can exist in two forms (enantiomers) that are mirror images of each other. This subtle difference has tremendously important implications in chemistry, as two enantiomers can exhibit completely different or even opposite biological or pharmacological properties. Similarly, the mechanical, magnetic or electrical properties of many materials can vary completely depending on whether they are made up of a single enantiomer or mixtures of enantiomers. As a consequence of all this, there is a real need at both laboratory and industrial level for synthetic procedures that allow chiral compounds to be obtained selectively in a defined enantiomeric form. Among the different methodologies available for this purpose, those using chiral catalysts are the most suitable, as they allow minimising the consumption of chiral starting materials and reducing waste production, contributing to more efficient, more economical and more environmentally friendly chemical processes. In this context, the asymmetric catalysis group investigates the development of new chiral catalysts based on both metal complexes and organocatalysts and their application in various enantioselective C-C bond formation reactions aimed at the synthesis of enantiomerically enriched chiral organic compounds of pharmacological interest. These reactions include functionalisation reactions of aromatic and heteroaromatic compounds (Friedel-Crafts reactions), carbanion addition reactions (aldol reactions, Henry reactions), addition reactions of organometallic reagents (alkylation and alkynylation) or cycloaddition reactions (Diels-Alder reactions, 1,3-dipolar addition) etc. We have recently incorporated the use of photoredox catalysis in C-C bond formation reactions.
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Web:
 
Scientific-technical goals:
  • Desarrollo de nuevas metodologias de formacion de enlaces C-C mediante catalisis asimetrica
  • Desarrollo de nuevos catalizadores quirales basados en complejos metalicos y organocatalizadores
  • Sintesis enantioselectiva de compuestos de interes farmacologico y agroquimico utilizando catalisis enantioselectiva
  • Desarrollo de nuevas metodologias de formacion de enlaces C-C mediante catalisis fotorredox.
 
Research lines:
  • Development of new asymmetric catalytic methodologies for C-C bond formation.Use of chiral catalysts (metal complexes and organocatalysts) in new reactions of interest in organic synthesis in which C-C bonds and stereogenic centres are generated simultaneously. Synthesis of chiral building blocks.
  • Development of new chiral catalysts.Design and synthesis of new chiral ligands capable of forming complexes with metal ions useful as chiral catalysts (Lewis acids). Design and synthesis of new chiral organic catalysts by proton transfer, hydrogen bridge formation or phase transfer.
  • Enantioselective synthesis of products with biological and pharmacological interest.Enantioselective synthesis of compounds with known or potential biological or pharmacological activity by chemical transformation of chiral products obtained by asymmetric catalysis.
 
Group members:
Name Nature of participation Entity Description
GONZALO BLAY LLINARESDirectorUniversitat de València
Research team
MARIA LUZ CARDONA PROSPERMemberUniversitat de València - Estudi GeneralUVEG honorary professor
JOSE RAMON PEDRO LLINARESMemberUniversitat de València
CARLOS VILA DESCALSMemberUniversitat de València
MARC MONTESINOS MAGRANERMemberUniversitat de València
ALICIA MONLEON VENTURAMemberUniversitat de València
AMPARO SANZ MARCOMemberUniversitat de València
 
CNAE:
  • -
 
Associated structure:
  • Organic Chemistry
 
Keywords:
  • Síntesis enantioselectiva; Friedel-Crafts; Alquilación; Alquinilación; Reacción de Henry; Reacciones de cicloadición
  • ligandos quirales; metales de transición; organocatalizadores, ácidos de Lewis quirales; transferencia de protón; puente de hidrógeno; PTC
  • Indoles; pirroles; heterociclos; aminoalcoholes; aril etanol aminas