What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
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.
His most cited work include:
- Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water (283 citations)
- A theoretical study on the mechanism of the thermal and the acid-catalyzed decarboxylation of 2-oxetanones (.beta.-lactones) (270 citations)
- A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure. (192 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Organic chemistry (42.70%)
- Enantioselective synthesis (42.70%)
- Catalysis (35.84%)
What were the highlights of his more recent work (between 2013-2021)?
- Catalysis (35.84%)
- Organic chemistry (42.70%)
- Enantioselective synthesis (42.70%)
In recent papers he was focusing on the following fields of study:
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.
Between 2013 and 2021, his most popular works were:
- Light‐Driven Organocatalysis Using Inexpensive, Nontoxic Bi2O3 as the Photocatalyst (94 citations)
- Conversion of oxiranes and CO2 to organic cyclic carbonates using a recyclable, bifunctional polystyrene-supported organocatalyst (89 citations)
- Organocatalysis on Tap: Enantioselective Continuous Flow Processes Mediated by Solid‐Supported Chiral Organocatalysts (74 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
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.
