Her primary scientific interests are in Enantioselective synthesis, Catalysis, Stereochemistry, Organic chemistry and Ligand. Her studies in Enantioselective synthesis integrate themes in fields like Medicinal chemistry, Palladium, Allylic rearrangement, Oxazoline and Thioether. Her Allylic rearrangement research is multidisciplinary, incorporating elements of Nucleophile and Substitution reaction.
Montserrat Diéguez combines subjects such as Diphosphines, Carbohydrate derivative and DuPhos with her study of Stereochemistry. She has included themes like Combinatorial chemistry, Moiety and Stereocenter in her Ligand study. Her Asymmetric hydrogenation study integrates concerns from other disciplines, such as Noyori asymmetric hydrogenation and Phosphine.
Her primary areas of study are Catalysis, Organic chemistry, Enantioselective synthesis, Ligand and Combinatorial chemistry. Many of her studies involve connections with topics such as Medicinal chemistry and Catalysis. Her work in the fields of Enantioselective synthesis, such as Enantiomeric excess, overlaps with other areas such as Conjugate.
Her Ligand research is multidisciplinary, relying on both Substituent, Moiety and Stereochemistry. Her Stereochemistry study combines topics from a wide range of disciplines, such as Stereocenter, Allylic rearrangement, Tsuji–Trost reaction and Substitution reaction. Her research in Combinatorial chemistry tackles topics such as Transfer hydrogenation which are related to areas like Thioamide.
Montserrat Diéguez mainly focuses on Catalysis, Asymmetric hydrogenation, Combinatorial chemistry, Ligand and Iridium. Her Catalysis research is classified as research in Organic chemistry. Her biological study spans a wide range of topics, including Thioether, Molecule, Allylic rearrangement and Enantioselective synthesis.
Her study in Allylic rearrangement is interdisciplinary in nature, drawing from both Stereochemistry and Substitution reaction. Her study explores the link between Enantioselective synthesis and topics such as Steric effects that cross with problems in Aryl. Her Ligand study combines topics from a wide range of disciplines, such as Alkene and Nucleophile.
The scientist’s investigation covers issues in Catalysis, Asymmetric hydrogenation, Organic chemistry, Substrate and Iridium. Montserrat Diéguez is interested in Oxazoline, which is a field of Catalysis. Her research in Oxazoline intersects with topics in Stereocenter, Indene, Reaction conditions, Stereochemistry and Nucleophile.
Asymmetric hydrogenation is a subfield of Enantioselective synthesis that Montserrat Diéguez tackles. Her Enantioselective synthesis research integrates issues from Methylene, Medicinal chemistry, Moiety, Alkene and Chirality. Her Iridium research is multidisciplinary, incorporating perspectives in Rhodium and Polymer chemistry.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Enantioselective Copper-Catalyzed Conjugate Addition and Allylic Substitution Reactions
Alexandre Alexakis;Jan E. Bäckvall;Norbert Krause;Oscar Pàmies.
Chemical Reviews (2008)
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)
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)
Chiral thioether ligands: coordination chemistry and asymmetric catalysis
Anna M Masdeu-Bultó;Montserrat Diéguez;Erika Martin;Montserrat Gómez.
Coordination Chemistry Reviews (2003)
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)
Recent advances in Rh-catalyzed asymmetric hydroformylation using phosphite ligands
Montserrat Diéguez;Oscar Pàmies;Carmen Claver.
Tetrahedron-asymmetry (2004)
Chiral diphosphites derived from D-glucose: new ligands for the asymmetric catalytic hydroformylation of vinyl arenes.
Montserrat Diéguez;Oscar Pàmies;Aurora Ruiz;Sergio Castillón.
Chemistry: A European Journal (2001)
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