What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of study are Organic chemistry, Catalysis, Palladium, Pincer movement and Combinatorial chemistry.
His Regioselectivity, Reagent, Allylic rearrangement, Borylation and Hypervalent molecule investigations are all subjects of Organic chemistry research.
In general Catalysis study, his work on Homogeneous catalysis often relates to the realm of Substrate, thereby connecting several areas of interest.
His Palladium research is multidisciplinary, relying on both Medicinal chemistry and Coupling reaction.
His study in the field of POCOP also crosses realms of Surface modification.
His study in Combinatorial chemistry is interdisciplinary in nature, drawing from both Electrophile, Organic synthesis and Enantioselective synthesis.
His most cited work include:
- Catalysis by Palladium Pincer Complexes (585 citations)
- Electrophilic Trifluoromethylation by Copper-Catalyzed Addition of CF3-Transfer Reagents to Alkenes and Alkynes (209 citations)
- Pincer Complex-Catalyzed Allylation of Aldehyde and Imine Substrates via Nucleophilic η1-Allyl Palladium Intermediates (129 citations)
What are the main themes of his work throughout his whole career to date?
Catalysis, Palladium, Organic chemistry, Medicinal chemistry and Allylic rearrangement are his primary areas of study.
His Catalysis research is multidisciplinary, incorporating perspectives in Combinatorial chemistry and Borylation.
The concepts of his Palladium study are interwoven with issues in Electrophile, Coupling reaction, Regioselectivity, Aldehyde and Silylation.
His study on Medicinal chemistry also encompasses disciplines like
- Moiety which intersects with area such as Substituent,
- Ligand and related Photochemistry.
His Allylic rearrangement study combines topics from a wide range of disciplines, such as Substitution reaction, Electrophilic substitution and Nucleophilic substitution.
His studies in Pincer movement integrate themes in fields like Polymer chemistry, Enantioselective synthesis and Imine.
He most often published in these fields:
- Catalysis (51.75%)
- Palladium (45.80%)
- Organic chemistry (43.36%)
What were the highlights of his more recent work (between 2015-2021)?
- Catalysis (51.75%)
- Organic chemistry (43.36%)
- Reagent (16.43%)
In recent papers he was focusing on the following fields of study:
Kálmán J. Szabó mainly focuses on Catalysis, Organic chemistry, Reagent, Medicinal chemistry and Combinatorial chemistry.
The Palladium, Stereocenter and Stereoselectivity research he does as part of his general Catalysis study is frequently linked to other disciplines of science, such as Coupling, therefore creating a link between diverse domains of science.
His study ties his expertise on Alkene together with the subject of Palladium.
His work deals with themes such as Trifluoromethylation, Electrophile, Fluorine and Reaction mechanism, which intersect with Reagent.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Aryl, Propargyl, Allylic rearrangement and Regioselectivity.
Kálmán J. Szabó has included themes like Selectivity and Benziodoxole in his Combinatorial chemistry study.
Between 2015 and 2021, his most popular works were:
- Recent Advances in the Preparation and Application of Allylboron Species in Organic Synthesis (85 citations)
- Rhodium-Catalyzed Geminal Oxyfluorination and Oxytrifluoro-Methylation of Diazocarbonyl Compounds. (59 citations)
- Fluorinative ring-opening of cyclopropanes by hypervalent iodine reagents. An efficient method for 1,3-oxyfluorination and 1,3-difluorination (47 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His scientific interests lie mostly in Reagent, Organic chemistry, Catalysis, Electrophile and Allylic rearrangement.
His Reagent research incorporates themes from Combinatorial chemistry and Photochemistry.
Kálmán J. Szabó merges many fields, such as Organic chemistry and Onium, in his writings.
His Catalysis study focuses on Stereoselectivity in particular.
His Electrophile research is multidisciplinary, relying on both Organocatalysis, Stereocenter, Enantioselective synthesis, Indole test and Reaction mechanism.
His Allylic rearrangement research is multidisciplinary, incorporating perspectives in Palladium, Transition metal, Adduct, Alkene and Cyclohexanol.
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