What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
The scientist’s investigation covers issues in Organic chemistry, Catalysis, Aryl, Palladium and Combinatorial chemistry.
His study in Amination, Yield, Copper catalyzed, Phosphine and Suzuki reaction falls under the purview of Organic chemistry.
His Catalysis study combines topics in areas such as Halide, Molecule, Polymer chemistry and Copper.
His Aryl research is multidisciplinary, incorporating perspectives in Medicinal chemistry, Coupling reaction, Oxidative addition, Ligand and Substrate.
His research investigates the connection with Palladium and areas like Photochemistry which intersect with concerns in C c coupling.
Stephen L. Buchwald has included themes like Intramolecular reaction, Intramolecular force, Diamine and Cascade reaction in his Combinatorial chemistry study.
His most cited work include:
- Palladium-Catalyzed Suzuki-Miyaura Cross-coupling Reactions Employing Dialkylbiaryl Phosphine Ligands (1626 citations)
- Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination (1406 citations)
- Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation (1318 citations)
What are the main themes of his work throughout his whole career to date?
Stephen L. Buchwald mainly investigates Catalysis, Organic chemistry, Aryl, Combinatorial chemistry and Palladium.
Stephen L. Buchwald combines subjects such as Ligand, Medicinal chemistry and Polymer chemistry with his study of Catalysis.
His work in Molecule, Yield, Copper, Copper catalyzed and Regioselectivity are all subfields of Organic chemistry research.
His work deals with themes such as Coupling reaction, Halide, Bromide, Substrate and Reductive elimination, which intersect with Aryl.
His Combinatorial chemistry research is multidisciplinary, relying on both Reagent, Electrophile, Intramolecular force, Coupling and Nucleophile.
His research in Palladium intersects with topics in Oxidative addition, Photochemistry and Phosphine.
He most often published in these fields:
- Catalysis (63.54%)
- Organic chemistry (47.08%)
- Aryl (37.61%)
What were the highlights of his more recent work (between 2013-2021)?
- Catalysis (63.54%)
- Combinatorial chemistry (32.74%)
- Organic chemistry (47.08%)
In recent papers he was focusing on the following fields of study:
Stephen L. Buchwald spends much of his time researching Catalysis, Combinatorial chemistry, Organic chemistry, Palladium and Enantioselective synthesis.
His research integrates issues of Aryl, Copper hydride, Ligand and Medicinal chemistry in his study of Catalysis.
Stephen L. Buchwald has researched Aryl in several fields, including Halide, Reactivity, Substrate, Halogenation and Phosphine.
The various areas that Stephen L. Buchwald examines in his Combinatorial chemistry study include Reagent, Coupling reaction, Regioselectivity, Molecule and Nucleophile.
His research on Organic chemistry frequently links to adjacent areas such as Amino acid.
His Palladium research incorporates themes from Yield, Cysteine, Stereochemistry, Oxidative addition and Reductive elimination.
Between 2013 and 2021, his most popular works were:
- Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions (759 citations)
- Organometallic palladium reagents for cysteine bioconjugation (203 citations)
- Copper Hydride Catalyzed Hydroamination of Alkenes and Alkynes (198 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Catalysis, Organic chemistry, Combinatorial chemistry, Palladium and Aryl.
The concepts of his Catalysis study are interwoven with issues in Reagent, Molecule and Ligand.
His Combinatorial chemistry study integrates concerns from other disciplines, such as Yield, Weak base, Reactivity, Bond formation and Chemical space.
His biological study spans a wide range of topics, including Medicinal chemistry, Coupling reaction, Cysteine, Oxidative addition and Peptide.
His Aryl research includes elements of Nickel, Halide, Substrate, Substituent and Natural product.
His Amination study incorporates themes from Reaction conditions and Amine gas treating.
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