2012 - Fellow of the American Association for the Advancement of Science (AAAS)
His main research concerns Catalysis, Organic chemistry, Medicinal chemistry, Photochemistry and Enantioselective synthesis. His Catalysis research includes elements of Combinatorial chemistry, Intramolecular force and Molecule. The Combinatorial chemistry study which covers Homogeneous catalysis that intersects with Electrophilic addition and Platinum.
His Medicinal chemistry research is multidisciplinary, relying on both Aryl, Reactivity and Palladium. His study focuses on the intersection of Photochemistry and fields such as Chemical reaction with connections in the field of Ruthenium and Photocatalysis. While the research belongs to areas of Enantioselective synthesis, Michel R. Gagné spends his time largely on the problem of Stereochemistry, intersecting his research to questions surrounding Redox and Carbenium ion.
His primary areas of investigation include Catalysis, Organic chemistry, Medicinal chemistry, Stereochemistry and Combinatorial chemistry. He has included themes like Reactivity, Molecule and Polymer chemistry in his Catalysis study. His Medicinal chemistry study which covers Palladium that intersects with Photochemistry.
As part of the same scientific family, Michel R. Gagné usually focuses on Stereochemistry, concentrating on Enantioselective synthesis and intersecting with Bite angle and Allylic rearrangement. Michel R. Gagné interconnects Synthon, Homogeneous catalysis, Reactive intermediate, Cationic polymerization and Dichloromethane in the investigation of issues within Combinatorial chemistry. His Alkene study combines topics in areas such as Platinum and Olefin fiber.
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Organic chemistry, Stereochemistry and Medicinal chemistry. His Catalysis study frequently links to other fields, such as Aryl. Michel R. Gagné has researched Combinatorial chemistry in several fields, including Electrophile, Green chemistry, Synthon, Homogeneous catalysis and Reactivity.
In the subject of general Organic chemistry, his work in Deoxygenation and Monosaccharide is often linked to Identification, Selection and Protocol, thereby combining diverse domains of study. His Stereochemistry research incorporates elements of Non-covalent interactions and Stereoisomerism. He has researched Medicinal chemistry in several fields, including Oxidative addition, Xantphos, Reductive elimination and Silylation.
His primary scientific interests are in Catalysis, Combinatorial chemistry, Stereochemistry, Organic chemistry and Cycloisomerization. His Catalysis research is multidisciplinary, relying on both Molecule and Synthon. His Combinatorial chemistry research includes themes of Electrophile and Homogeneous catalysis.
His research investigates the link between Stereochemistry and topics such as Stereoisomerism that cross with problems in Moiety. His work in the fields of Organic chemistry, such as Deoxygenation, intersects with other areas such as Protocol and Selection. He interconnects Platinum, Enantioselective synthesis and Pincer ligand in the investigation of issues within Cycloisomerization.
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Organolanthanide-Catalyzed Hydroamination. A Kinetic, Mechanistic, and Diastereoselectivity Study of the Cyclization of N-Unprotected Amino Olefins
Michel R. Gagne;Charlotte L. Stern;Tobin J. Marks.
Journal of the American Chemical Society (1992)
Chiral Organolanthanides Designed for Asymmetric Catalysis. A Kinetic and Mechanistic Study of Enantioselective Olefin Hydroamination/Cyclization and Hydrogenation by C1-Symmetric Me2Si(Me4C5)(C5H3R*)Ln Complexes where R* = Chiral Auxiliary
Michael A. Giardello;Vincent P. Conticello;Laurent Brard;Michel R. Gagne.
Journal of the American Chemical Society (1994)
Application of Chiral Mixed Phosphorus/Sulfur Ligands to Palladium-Catalyzed Allylic Substitutions
David A. Evans;Kevin R. Campos;Jason S. Tedrow;Forrest E. Michael.
Journal of the American Chemical Society (2000)
Room‐Temperature Palladium‐Catalyzed C ? H Activation: ortho‐Carbonylation of Aniline Derivatives
Chris E. Houlden;Marc Hutchby;Chris D. Bailey;J. Gair Ford.
Angewandte Chemie (2009)
Organolanthanide-catalyzed hydroamination. Facile, regiospecific cyclization of unprotected amino olefins
Michel R. Gagné;Tobin J. Marks.
Journal of the American Chemical Society (1989)
Distinct reactivity of Pd(OTs)2: the intermolecular Pd(II)-catalyzed 1,2-carboamination of dienes.
Chris E. Houlden;Chris D. Bailey;J. Gair Ford;Michel R. Gagné.
Journal of the American Chemical Society (2008)
A chiral samarium-based catalyst for the asymmetric Meerwein-Ponndorf-Verley reduction
David A. Evans;Scott G. Nelson;Michel R. Gagne;Alexander R. Muci.
Journal of the American Chemical Society (1993)
Mechanistic Surprises in the Gold(I)‐Catalyzed Intramolecular Hydroarylation of Allenes
Dieter Weber;Michael A. Tarselli;Michel R. Gagné.
Angewandte Chemie (2009)
Electrophilic Activation of Alkenes by Platinum(II): So Much More Than a Slow Version of Palladium(II)
Anthony R. Chianese;Stephen J. Lee;Michel R. Gagné.
Angewandte Chemie (2007)
Intermolecular Addition of Glycosyl Halides to Alkenes Mediated by Visible Light
R. Stephen Andrews;Jennifer J. Becker;Michel R. Gagné.
Angewandte Chemie (2010)
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