2023 - Research.com Chemistry in United States Leader Award
2022 - Research.com Best Scientist Award
2022 - Research.com Chemistry in United States Leader Award
2019 - Wolf Prize in Chemistry, Wolf Foundation for pioneering the development of transition metal catalyzed procedures that are broadly applicable and allow carbon-heteroatom bonds of all sorts to be formed with previously unknown efficiency and precision.
2018 - Tetrahedron Prize for Creativity in Organic Chemistry or Bioorganic and Medicinal Chemistry, Elsevier
2016 - William H. Nichols Medal, American Chemical Society (ACS)
2014 - BBVA Foundation Frontiers of Knowledge Award
2014 - Linus Pauling Award, American Chemical Society (ACS)
2013 - Arthur C. Cope Award, American Chemical Society (ACS)
2008 - Member of the National Academy of Sciences
2000 - Fellow of the American Academy of Arts and Sciences
1997 - Fellow of the American Association for the Advancement of Science (AAAS)
1988 - Fellow of Alfred P. Sloan Foundation
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.
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.
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.
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.
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.
Palladium-Catalyzed Suzuki-Miyaura Cross-coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
Ruben Martin;Stephen L. Buchwald.
Accounts of Chemical Research (2008)
Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation
John P. Wolfe;Seble Wagaw;§ and Jean-François Marcoux;Stephen L. Buchwald.
Accounts of Chemical Research (1998)
Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination
David S. Surry;Stephen L. Buchwald.
Angewandte Chemie (2008)
Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
Timothy E Barder;Shawn D Walker;Joseph R Martinelli;Stephen L Buchwald.
Journal of the American Chemical Society (2005)
Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
Paula Ruiz-Castillo;Stephen Leffler Buchwald.
Chemical Reviews (2016)
Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.
David S. Surry;Stephen Leffler Buchwald.
Chemical Science (2011)
Practical Palladium Catalysts for C-N and C-O Bond Formation
Alex R. Muci;Stephen L. Buchwald.
Topics in Current Chemistry (2002)
Highly Active Palladium Catalysts for Suzuki Coupling Reactions
John P. Wolfe;Robert A. Singer;Bryant H. Yang;Stephen L. Buchwald.
Journal of the American Chemical Society (1999)
A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines
Anil S. Guram;Roger A. Rennels;Stephen L. Buchwald.
Angewandte Chemie (1995)
A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides
David W. Old;John P. Wolfe;Stephen L. Buchwald.
Journal of the American Chemical Society (1998)
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