What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
His primary scientific interests are in Organic chemistry, Biochemistry, Primary biliary cirrhosis, Pyruvate dehydrogenase complex and Cystic fibrosis transmembrane conductance regulator.
The Organic chemistry study which covers Solid-phase synthesis that intersects with Stereoselectivity and Isoquinoline.
His Biochemistry research is multidisciplinary, incorporating elements of Transfection and Cell biology.
The Primary biliary cirrhosis study combines topics in areas such as Autoantibody and Molecular mimicry.
The various areas that he examines in his Pyruvate dehydrogenase complex study include Antibody, Hapten and Peptide.
His work carried out in the field of Cystic fibrosis transmembrane conductance regulator brings together such families of science as Chloride channel, Flavones, Ion transporter and Cyclic nucleotide-binding domain.
His most cited work include:
- Chemical inhibition of the mitochondrial division dynamin reveals its role in Bax/Bak-dependent mitochondrial outer membrane permeabilization. (760 citations)
- "Analogous" Organic Synthesis of Small-Compound Libraries: Validation of Combinatorial Chemistry in Small-Molecule Synthesis (261 citations)
- Mechanism-based corrector combination restores ΔF508-CFTR folding and function (255 citations)
What are the main themes of his work throughout his whole career to date?
Mark J. Kurth focuses on Organic chemistry, Stereochemistry, Combinatorial chemistry, Cycloaddition and Medicinal chemistry.
Mark J. Kurth frequently studies issues relating to Solid-phase synthesis and Organic chemistry.
His biological study spans a wide range of topics, including Electrophile, Asymmetric induction, Cystic fibrosis transmembrane conductance regulator and Stereoselectivity.
His Cycloaddition research is multidisciplinary, incorporating perspectives in Hydantoin, Intramolecular force and Nitrile.
His Nitrile research integrates issues from Oxide and 1,3-Dipolar cycloaddition.
His research on Medicinal chemistry frequently links to adjacent areas such as Ring.
He most often published in these fields:
- Organic chemistry (30.79%)
- Stereochemistry (22.25%)
- Combinatorial chemistry (17.30%)
What were the highlights of his more recent work (between 2011-2021)?
- Combinatorial chemistry (17.30%)
- Organic chemistry (30.79%)
- Davis–Beirut reaction (2.92%)
In recent papers he was focusing on the following fields of study:
Mark J. Kurth mainly investigates Combinatorial chemistry, Organic chemistry, Davis–Beirut reaction, Cycloaddition and Catalysis.
His Combinatorial chemistry study incorporates themes from Quinoline, Stereochemistry and Substrate.
His specific area of interest is Organic chemistry, where he studies Isoxazole.
Mark J. Kurth interconnects Nitrile, Intramolecular force and Azide in the investigation of issues within Cycloaddition.
His Catalysis study integrates concerns from other disciplines, such as Photochemistry and Aryl.
His Potentiator research includes elements of Biochemistry and Cystic fibrosis transmembrane conductance regulator.
Between 2011 and 2021, his most popular works were:
- Mechanism-based corrector combination restores ΔF508-CFTR folding and function (255 citations)
- One-pot–Two-step Cascade Synthesis of Quinazolinotriazolobenzodiazepines (52 citations)
- Multicomponent Assembly of Highly Substituted Indoles by Dual Palladium‐Catalyzed Coupling Reactions (48 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of study are Biochemistry, Molecule, Cycloaddition, Catalysis and Cystic fibrosis transmembrane conductance regulator.
His studies in Biochemistry integrate themes in fields like Autoantibody and Innate immune system.
His Molecule research is within the category of Organic chemistry.
His work deals with themes such as Combinatorial chemistry, Small Molecule Libraries, Stereochemistry and Nitrile, which intersect with Cycloaddition.
His Stereochemistry study combines topics from a wide range of disciplines, such as Biological activity and Adenosine.
His Cystic fibrosis transmembrane conductance regulator research incorporates themes from EC50, Potency, Structure–activity relationship and Moiety.
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