2017 - Bader Award, Royal Society of Chemistry (UK)
Organic chemistry, Catalysis, Palladium, Aryl and Photochemistry are his primary areas of study. His biological study spans a wide range of topics, including Combinatorial chemistry and Medicinal chemistry. A large part of his Catalysis studies is devoted to Regioselectivity.
His Palladium research focuses on Molecule and how it relates to Computational chemistry, Alkylation and Stoichiometry. His research integrates issues of Electrophile, Polymer chemistry, Homogeneous catalysis and Stereoisomerism in his study of Aryl. Michael F. Greaney has included themes like Trimethylsilyl, Silane, Halobenzene and Wittig reaction in his Aryne study.
His scientific interests lie mostly in Organic chemistry, Catalysis, Combinatorial chemistry, Aryne and Medicinal chemistry. Michael F. Greaney combines subjects such as Aryl and Polymer chemistry with his study of Catalysis. His Aryl study integrates concerns from other disciplines, such as Stoichiometry and Smiles rearrangement.
His Combinatorial chemistry research is multidisciplinary, incorporating perspectives in Molecule, Stereochemistry, Regioselectivity and Suzuki reaction. In his research, Trifluoromethanesulfonate is intimately related to Trimethylsilyl, which falls under the overarching field of Aryne. His Medicinal chemistry study combines topics in areas such as Indole test, Ring and Nucleophile.
Michael F. Greaney mainly investigates Catalysis, Combinatorial chemistry, Organic chemistry, Aryl and Smiles rearrangement. The various areas that Michael F. Greaney examines in his Catalysis study include Reagent and Polymer chemistry. His Combinatorial chemistry study combines topics from a wide range of disciplines, such as In situ, Regioselectivity, Indole test, Biochemistry and Molecule.
Many of his studies on Organic chemistry involve topics that are commonly interrelated, such as Medicinal chemistry. His research on Smiles rearrangement also deals with topics like
Michael F. Greaney mostly deals with Organic chemistry, Catalysis, Combinatorial chemistry, Aryl and Halogenation. His research related to Aryne, Stoichiometry, Metal free and Smiles rearrangement might be considered part of Organic chemistry. His work on Regioselectivity as part of general Catalysis research is frequently linked to Visible spectrum, thereby connecting diverse disciplines of science.
His work deals with themes such as In situ, Domino and Group, which intersect with Combinatorial chemistry. His Aryl study incorporates themes from Electrophile, Heteroatom, Medicinal chemistry, Steric effects and Reaction conditions. His Halogenation research is multidisciplinary, relying on both Indole test, Enzyme, Stereoisomerism and Ruthenium.
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Direct Arylation of Thiazoles on Water
Gemma L. Turner;James A. Morris;Michael F. Greaney.
Angewandte Chemie (2007)
Decarboxylative C-H cross-coupling of azoles.
Fengzhi Zhang;Michael F. Greaney.
Angewandte Chemie (2010)
Ruthenium-Catalyzed meta-Selective C-H Bromination
Christopher J. Teskey;Andrew Y. W. Lui;Michael F. Greaney.
Angewandte Chemie (2015)
Photocycloaddition in natural product synthesis
Jone Iriondo‐Alberdi;Michael F. Greaney.
European Journal of Organic Chemistry (2007)
Atom-Economical Transformation of Diaryliodonium Salts: Tandem C–H and N–H Arylation of Indoles
Sachin G. Modha;Michael F. Greaney.
Journal of the American Chemical Society (2015)
Intramolecular oxidative C-H coupling for medium-ring synthesis
Didier G. Pintori;Michael F. Greaney.
Journal of the American Chemical Society (2011)
Direct arylations on water: synthesis of 2,5-disubstituted oxazoles balsoxin and texaline
Stephan A. Ohnmacht;Patrizia Mamone;Andrew J. Culshaw;Michael F. Greaney.
Chemical Communications (2008)
Nucleophilic catalysis of acylhydrazone equilibration for protein-directed dynamic covalent chemistry
Venugopal T. Bhat;Anne M. Caniard;Torsten Luksch;Ruth Brenk.
Nature Chemistry (2010)
Three-Component Azidation of Styrene-Type Double Bonds: Light-Switchable Behavior of a Copper Photoredox Catalyst.
Gabriele Fumagalli;Pauline T. G. Rabet;Scott Boyd;Michael F. Greaney.
Angewandte Chemie (2015)
Direct arylations of 2H-indazoles on water.
Stephan A. Ohnmacht;Andrew J. Culshaw;Michael F. Greaney.
Organic Letters (2010)
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