2020 - Fellow of the American Chemical Society
2012 - Fellow of Alfred P. Sloan Foundation
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Organic chemistry, Enantioselective synthesis and Stereochemistry. Catalysis is closely attributed to Aryl in her research. Her research combines Aqueous solution and Combinatorial chemistry.
Her work in Enantioselective synthesis addresses subjects such as Stereoisomerism, which are connected to disciplines such as Catalytic method and Halogenation. Her studies deal with areas such as Halide, Squaramide, Thiourea organocatalysis and Hydrogen bond as well as Stereochemistry. Her Photoredox catalysis research incorporates themes from Dimethylaniline, Chlorine, Alkyl and Nickel.
Abigail G. Doyle mostly deals with Catalysis, Enantioselective synthesis, Organic chemistry, Nickel and Combinatorial chemistry. Her work carried out in the field of Catalysis brings together such families of science as Photochemistry, Aryl, Reagent and Polymer chemistry. Her Enantioselective synthesis research is multidisciplinary, incorporating elements of Ion, Alkylation, Stereochemistry and Nucleophile.
Her Organic chemistry study deals with Medicinal chemistry intersecting with Lewis acid catalysis, Desymmetrization and Kinetic resolution. Her research in Nickel intersects with topics in Pyridine, Suzuki reaction, Pyridinium, Molecule and Bond formation. Her Combinatorial chemistry research incorporates elements of Electrophile, Negishi coupling, Ligand, Alkyl and Phenethylamines.
Catalysis, Photoredox catalysis, Aryl, Set and Photochemistry are her primary areas of study. Her research on Catalysis frequently links to adjacent areas such as Polymer chemistry. The various areas that Abigail G. Doyle examines in her Aryl study include Methyl radical, Electrophile and Trimethyl orthoformate.
The Methyl radical study combines topics in areas such as Reagent, Reaction conditions, Medicinal chemistry and Nickel. Her Electrophile research includes elements of Regioselectivity, Coupling reaction, Epoxide, Combinatorial chemistry and Phenethylamines. In the subject of general Alkyl, her work in Aryl halide is often linked to Coupling, thereby combining diverse domains of study.
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.
Small-molecule H-bond donors in asymmetric catalysis.
Abigail Gutmann Doyle;Eric N. Jacobsen.
Chemical Reviews (2007)
Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp3-carbons with aryl halides
Zhiwei Zuo;Derek T. Ahneman;Lingling Chu;Jack A. Terrett.
Science (2014)
A synthetically useful, self-assembling MMO mimic system for catalytic alkene epoxidation with aqueous H2O2.
M. Christina White;and Abigail G. Doyle;Eric N. Jacobsen.
Journal of the American Chemical Society (2001)
Enantioselective Thiourea-Catalyzed Additions to Oxocarbenium Ions
Sarah E. Reisman;Abigail G. Doyle;Eric N. Jacobsen.
Journal of the American Chemical Society (2008)
Predicting reaction performance in C–N cross-coupling using machine learning
Derek T. Ahneman;Jesús G. Estrada;Shishi Lin;Spencer D. Dreher.
Science (2018)
The chemistry of transition metals with three-membered ring heterocycles.
Chung-Yang Dennis Huang;Abigail G Doyle.
Chemical Reviews (2014)
Direct C(sp3)-H Cross Coupling Enabled by Catalytic Generation of Chlorine Radicals.
Benjamin J. Shields;Abigail G. Doyle.
Journal of the American Chemical Society (2016)
Enantioselective ring opening of epoxides by fluoride anion promoted by a cooperative dual-catalyst system.
Julia A. Kalow;Abigail Gutmann Doyle.
Journal of the American Chemical Society (2010)
Palladium-Catalyzed Asymmetric Synthesis of Allylic Fluorides
Matthew H. Katcher;Abigail G. Doyle.
Journal of the American Chemical Society (2010)
PyFluor: A Low-Cost, Stable, and Selective Deoxyfluorination Reagent
Matthew K. Nielsen;Christian R. Ugaz;Wenping Li;Abigail G. Doyle.
Journal of the American Chemical Society (2015)
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