His primary areas of investigation include Organic chemistry, Catalysis, Combinatorial chemistry, Nickel and Aryne. His Organic chemistry research is mostly focused on the topic Aryl. His research in Catalysis focuses on subjects like Amide, which are connected to Synthon and Nucleophile.
His research ties Natural product and Combinatorial chemistry together. His Nickel study combines topics in areas such as Carbon, Oxygen and Palladium. The concepts of his Aryne study are interwoven with issues in Computational chemistry, Molecule and Regioselectivity.
His scientific interests lie mostly in Organic chemistry, Combinatorial chemistry, Catalysis, Stereochemistry and Total synthesis. All of his Organic chemistry and Molecule, Phenol and Reagent investigations are sub-components of the entire Organic chemistry study. His Combinatorial chemistry research includes elements of Ketone, Aryne, Electrophile and Ring.
His Catalysis research includes themes of Aryl, Nickel and Amide. The various areas that Neil K. Garg examines in his Stereochemistry study include Chemical synthesis, Stereocenter, Isothiocyanate and Stereoisomerism. His research in Total synthesis intersects with topics in Natural product and Bicyclic molecule.
Neil K. Garg mostly deals with Combinatorial chemistry, Catalysis, Stereochemistry, Stereocenter and Organic chemistry. His Combinatorial chemistry research incorporates themes from Substrate, Ketone, Chemical synthesis, Trifluoromethanesulfonate and Silylation. His Catalysis research integrates issues from Computational chemistry, Glovebox, Nickel and Amide.
His research in the fields of Total synthesis overlaps with other disciplines such as Nucleobase. His study in Total synthesis is interdisciplinary in nature, drawing from both Molecule and Alkaloid. In the subject of general Organic chemistry, his work in 8-Hydroxygeraniol and McFadyen–Stevens reaction is often linked to Student engagement, Chemistry education and Reputation, thereby combining diverse domains of study.
His primary areas of study are Combinatorial chemistry, Catalysis, Stereocenter, Stereochemistry and Stereoselectivity. His Combinatorial chemistry research is multidisciplinary, incorporating elements of Aryne, Negishi coupling, Catalytic cycle, Substrate and Nucleophile. His studies in Substrate integrate themes in fields like Electrophile, Nickel, Sequence, Amide and Ketone.
His research on Catalysis often connects related areas such as Polymer chemistry. His study looks at the relationship between Stereocenter and topics such as Chemical synthesis, which overlap with Diels alder, Ring, Aqueous medium and Enzyme binding. Stereochemistry is closely attributed to Stereoisomerism in his research.
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Nickel-Catalyzed Cross-Couplings Involving Carbon-Oxygen Bonds
Brad M. Rosen;Kyle W. Quasdorf;Daniella A. Wilson;Na Zhang.
Chemical Reviews (2011)
Conversion of amides to esters by the nickel-catalysed activation of amide C-N bonds
Liana Hie;Noah F. Fine Nathel;Tejas K. Shah;Emma L. Baker.
Suzuki–Miyaura Coupling of Aryl Carbamates, Carbonates, and Sulfamates
Kyle W. Quasdorf;Michelle Riener;Krastina V. Petrova;Neil K. Garg.
Journal of the American Chemical Society (2009)
Cross-coupling reactions of aryl pivalates with boronic acids.
Kyle W. Quasdorf;Xia Tian;Neil K. Garg.
Journal of the American Chemical Society (2008)
Breaking Amides using Nickel Catalysis
Jacob E. Dander;Neil K. Garg.
ACS Catalysis (2017)
Nickel-catalysed Suzuki–Miyaura coupling of amides
Nicholas A. Weires;Emma L. Baker;Neil K. Garg.
Nature Chemistry (2016)
Ni- and Fe-Catalyzed Cross-Coupling Reactions of Phenol Derivatives
Tehetena Mesganaw;Neil K. Garg.
Organic Process Research & Development (2013)
Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.
Kyle W. Quasdorf;Aurora Antoft-Finch;Peng Liu;Amanda L. Silberstein.
Journal of the American Chemical Society (2011)
The First Total Synthesis of Dragmacidin D
Neil K. Garg;Richmond Sarpong;Brian M. Stoltz.
Journal of the American Chemical Society (2002)
The role of aryne distortions, steric effects, and charges in regioselectivities of aryne reactions.
Jose M Medina;Joel L Mackey;Neil K Garg;Kendall N Houk.
Journal of the American Chemical Society (2014)
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