Miquel A. Pericàs focuses on Catalysis, Enantioselective synthesis, Organic chemistry, Stereochemistry and Polystyrene. His work in the fields of Cycloaddition overlaps with other areas such as Linker. Miquel A. Pericàs interconnects Substituent and Aldehyde in the investigation of issues within Enantioselective synthesis.
His Organic chemistry and Michael reaction, Enantiomeric excess, Aldol reaction, Ligand and Heterogeneous catalysis investigations all form part of his Organic chemistry research activities. His Ligand research incorporates themes from Covalent bond and Alcohol. The study incorporates disciplines such as Bifunctional, Hydroxyproline, Diphenylprolinol and Proline in addition to Polystyrene.
The scientist’s investigation covers issues in Organic chemistry, Enantioselective synthesis, Catalysis, Stereochemistry and Combinatorial chemistry. His work carried out in the field of Enantioselective synthesis brings together such families of science as Alcohol and Regioselectivity. His Catalysis study combines topics from a wide range of disciplines, such as Polystyrene, Ligand and Polymer chemistry.
Many of his studies involve connections with topics such as Medicinal chemistry and Stereochemistry. His Enantiopure drug study combines topics in areas such as Amino acid and Aryl. His Cycloaddition study incorporates themes from Azide and Alkyne.
His primary areas of investigation include Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Organocatalysis. His work deals with themes such as Photochemistry and Adduct, which intersect with Catalysis. His research related to Polystyrene, Michael reaction, Yield, Bifunctional and Phosphoric acid might be considered part of Organic chemistry.
His research in Enantioselective synthesis intersects with topics in Aldol reaction and Stereoselectivity. His Combinatorial chemistry research is multidisciplinary, incorporating elements of Heterogeneous catalysis and Ligand, Phosphinite. His studies in Ligand integrate themes in fields like Thioether, Allylic rearrangement, Substrate and Regioselectivity.
Miquel A. Pericàs mainly investigates Catalysis, Organic chemistry, Enantioselective synthesis, Cycloaddition and Polystyrene. The concepts of his Catalysis study are interwoven with issues in Combinatorial chemistry, Photochemistry, Thiourea and Hydrogen bond. In his works, Miquel A. Pericàs conducts interdisciplinary research on Organic chemistry and Rapid access.
Miquel A. Pericàs has researched Enantioselective synthesis in several fields, including Stereochemistry and Michael reaction. His studies deal with areas such as Regioselectivity, Annulation, Alkyne, Tris and Azide as well as Cycloaddition. His Tris research is multidisciplinary, incorporating perspectives in Ligand and Methanol.
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.
Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water
Daniel Font;Ciril Jimeno;Miquel A Pericàs.
Organic Letters (2006)
A theoretical study on the mechanism of the thermal and the acid-catalyzed decarboxylation of 2-oxetanones (.beta.-lactones)
Albert Moyano;Miquel A. Pericas;Eduard Valenti.
Journal of Organic Chemistry (1989)
A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure.
Salih Özçubukçu;Erhan Ozkal;Ciril Jimeno;Miquel A. Pericàs.
Organic Letters (2009)
Toward an Artificial Aldolase
Daniel Font;Sonia Sayalero;Amaia Bastero;Ciril Jimeno.
Organic Letters (2008)
Highly enantioselective Michael additions in water catalyzed by a PS-supported pyrrolidine.
Esther Alza;Xacobe C. Cambeiro;Ciril Jimeno;Miquel A. Pericàs.
Organic Letters (2007)
2-Piperidino-1,1,2-triphenylethanol: A Highly Effective Catalyst for the Enantioselective Arylation of Aldehydes
Montserrat Fontes;Xavier Verdaguer;Lluis Sola;Miquel A. Pericas.
Journal of Organic Chemistry (2004)
Functionalized nanoparticles as catalysts for enantioselective processes.
Sarabindu Roy;Miquel A. Pericàs.
Organic and Biomolecular Chemistry (2009)
A Solid‐Supported Organocatalyst for Highly Stereoselective, Batch, and Continuous‐Flow Mannich Reactions
Esther Alza;Carles Rodríguez-Escrich;Sonia Sayalero;Amaia Bastero.
Chemistry: A European Journal (2009)
Characterization of a (2R,3R)-2,3-butanediol dehydrogenase as the Saccharomyces cerevisiae YAL060W gene product. Disruption and induction of the gene.
Eva Gonzalez;Maria R. Fernandez;Carol Larroy;Lluis Sola.
Journal of Biological Chemistry (2000)
A solid-supported organocatalyst for continuous-flow enantioselective aldol reactions.
Carles Ayats;Andrea H. Henseler;Miquel A. Pericàs.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: