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.
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
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.
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.
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.
Catalysis by Palladium Pincer Complexes
Nicklas Selander;Kálmán J. Szabó.
Chemical Reviews (2011)
Electrophilic Trifluoromethylation by Copper-Catalyzed Addition of CF3-Transfer Reagents to Alkenes and Alkynes
Pär G. Janson;Ibrahim Ghoneim;Nadia O. Ilchenko;Kálmán J. Szabó.
Organic Letters (2012)
Pincer Complex-Catalyzed Allylation of Aldehyde and Imine Substrates via Nucleophilic η1-Allyl Palladium Intermediates
Niclas Solin;Johan Kjellgren;Kálmán J. Szabó.
Journal of the American Chemical Society (2004)
Pincer and pincer-type complexes : applications in organic synthesis and catalysis
Kalman J. Szabo;Ola F. Wendt.
Palladium Pincer Complex Catalyzed Substitution of Vinyl Cyclopropanes, Vinyl Aziridines, and Allyl Acetates with Tetrahydroxydiboron. An Efficient Route to Functionalized Allylboronic Acids and Potassium Trifluoro(allyl)borates
Sara Sebelius;Vilhelm J. Olsson;Kálmán J. Szabó.
Journal of the American Chemical Society (2005)
Direct Boronation of Allyl Alcohols with Diboronic Acid Using Palladium Pincer-Complex Catalysis. A Remarkably Facile Allylic Displacement of the Hydroxy Group under Mild Reaction Conditions
Vilhelm J. Olsson;Sara Sebelius;Nicklas Selander;Kalman J. Szabo.
Journal of the American Chemical Society (2006)
Recent Advances in the Preparation and Application of Allylboron Species in Organic Synthesis
Colin Diner;Kálmán J. Szabó.
Journal of the American Chemical Society (2017)
Evidence for a ruthenium dihydride species as the active catalyst in the RuCl2(PPh3)-catalyzed hydrogen transfer reaction in the presence of base
Attila Aranyos;Gábor Csjernyik;Kálmán J. Szabó;Jan-E. Bäckvall.
Chemical Communications (1999)
Petasis Borono-Mannich reaction and allylation of carbonyl compounds via transient allyl boronates generated by palladium-catalyzed substitution of allyl alcohols. an efficient one-pot route to stereodefined alpha-amino acids and homoallyl alcohols.
Nicklas Selander;Andreas Kipke;Sara Sebelius;Kálmán J. Szabó.
Journal of the American Chemical Society (2007)
Palladium-Catalyzed Coupling of Allylboronic Acids with Iodobenzenes. Selective Formation of the Branched Allylic Product in the Absence of Directing Groups
Sara Sebelius;Vilhelm J. Olsson;Olov A. Wallner;Kálmán J. Szabó.
Journal of the American Chemical Society (2006)
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: