His main research concerns Organic chemistry, Catalysis, Enantioselective synthesis, Stereochemistry and Ligand. His Asymmetric hydrogenation, Iridium, Hydroformylation, Ruthenium and Rhodium investigations are all subjects of Catalysis research. His Enantioselective synthesis study combines topics in areas such as Substitution reaction, Allylic rearrangement, Oxazoline, Metal catalyst and Synergistic catalysis.
Oscar Pàmies has researched Substitution reaction in several fields, including Copper catalyzed and Kinetic control. His Stereochemistry research incorporates themes from Diphosphines, Carbohydrate derivative, DuPhos and Transition metal. In his study, Regioselectivity and Combinatorial chemistry is inextricably linked to Moiety, which falls within the broad field of Ligand.
Catalysis, Organic chemistry, Enantioselective synthesis, Ligand and Combinatorial chemistry are his primary areas of study. His study looks at the relationship between Catalysis and fields such as Substrate, as well as how they intersect with chemical problems. His Enantioselective synthesis research is multidisciplinary, incorporating elements of Steric effects, Allylic rearrangement, Phosphinite and Palladium.
His Ligand research includes elements of Substituent, Moiety, Stereochemistry, Medicinal chemistry and Sugar. His Stereochemistry research is multidisciplinary, relying on both Carbohydrate, Substitution reaction and Tsuji–Trost reaction. His studies deal with areas such as Denticity, Enantiopure drug and Thioether as well as Combinatorial chemistry.
His primary scientific interests are in Catalysis, Combinatorial chemistry, Asymmetric hydrogenation, Enantioselective synthesis and Ligand. His research on Catalysis concerns the broader Organic chemistry. His Asymmetric hydrogenation research integrates issues from Pyridine, Medicinal chemistry and Moiety.
His Enantioselective synthesis study integrates concerns from other disciplines, such as Steric effects, Reactivity and Palladium. His study in Ligand is interdisciplinary in nature, drawing from both Sugar and Alkene. His studies in Allylic rearrangement integrate themes in fields like Stereochemistry, Nucleophile and Substitution reaction.
Oscar Pàmies mostly deals with Catalysis, Organic chemistry, Asymmetric hydrogenation, Enantioselective synthesis and Ligand. His study focuses on the intersection of Catalysis and fields such as Substrate with connections in the field of Trifluoromethyl, Phosphinite and Enantiomeric excess. His work in the fields of Organic chemistry, such as Iridium, Selectivity and Transfer hydrogenation, overlaps with other areas such as Scope.
His Asymmetric hydrogenation study incorporates themes from Moiety, Alkene, Noyori asymmetric hydrogenation, Substituent and Thioether. His research integrates issues of Combinatorial chemistry and Nanotechnology in his study of Enantioselective synthesis. As a part of the same scientific study, Oscar Pàmies usually deals with the Ligand, concentrating on Stereochemistry and frequently concerns with Nucleophilic substitution and Stereospecificity.
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Enantioselective Copper-Catalyzed Conjugate Addition and Allylic Substitution Reactions
Alexandre Alexakis;Jan E. Bäckvall;Norbert Krause;Oscar Pàmies.
Chemical Reviews (2008)
Combination of enzymes and metal catalysts. A powerful approach in asymmetric catalysis.
Oscar Pamies;Jan-E. Bäckvall.
Chemical Reviews (2003)
Asymmetric Hydrogenation of Olefins Using Chiral Crabtree-type Catalysts: Scope and Limitations
J. Johan Verendel;Oscar Pàmies;Montserrat Diéguez;Pher G. Andersson;Pher G. Andersson;Pher G. Andersson.
Chemical Reviews (2014)
Phosphite-containing ligands for asymmetric catalysis.
Piet W. N. M. van Leeuwen;Paul C. J. Kamer;Carmen Claver;Oscar Pàmies.
Chemical Reviews (2011)
Studies on the mechanism of metal-catalyzed hydrogen transfer from alcohols to ketones.
Oscar Pàmies;Jan-E. Bäckvall.
Chemistry: A European Journal (2001)
Ligands derived from carbohydrates for asymmetric catalysis
Montserrat Diéguez;Oscar Pàmies;Carmen Claver.
Chemical Reviews (2004)
Biaryl phosphites: new efficient adaptative ligands for Pd-catalyzed asymmetric allylic substitution reactions.
Montserrat Diéguez;Oscar Pàmies.
Accounts of Chemical Research (2010)
Carbohydrate derivative ligands in asymmetric catalysis
Montserrat Diéguez;Oscar Pàmies;Aurora Ruiz;Yolanda Dı́az.
Coordination Chemistry Reviews (2004)
Chemoenzymatic dynamic kinetic resolution.
Oscar Pàmies;Jan-E Bäckvall.
Trends in Biotechnology (2004)
Pyranoside phosphite-oxazoline ligands for the highly versatile and enantioselective ir-catalyzed hydrogenation of minimally functionalized olefins. A combined theoretical and experimental study.
Javier Mazuela;Per-Ola Norrby;Pher G. Andersson;Pher G. Andersson;Oscar Pàmies.
Journal of the American Chemical Society (2011)
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