Michel Pfeffer mostly deals with Medicinal chemistry, Stereochemistry, Palladium, Organic chemistry and Alkyne. The concepts of his Medicinal chemistry study are interwoven with issues in Photochemistry, Intramolecular force and Regioselectivity. His Stereochemistry study combines topics in areas such as Chromium, Reactivity, Ligand and Electrophile.
His Palladium research integrates issues from Nuclear magnetic resonance spectroscopy, Aryl, Carbon and Molecule. His Organic chemistry course of study focuses on Polymer chemistry and Ring. His research integrates issues of Bicyclic molecule and Crystal structure in his study of Alkyne.
His scientific interests lie mostly in Medicinal chemistry, Stereochemistry, Palladium, Organic chemistry and Reactivity. Michel Pfeffer has included themes like Tertiary amine and Intramolecular force in his Medicinal chemistry study. His Stereochemistry research incorporates elements of Crystallography, Crystal structure, Ligand, Alkyne and Molecule.
The various areas that Michel Pfeffer examines in his Palladium study include Yield, Quinoline, Ring, Polymer chemistry and Carbon. Organic chemistry is a component of his Catalysis, Coupling reaction, Aryl and Reinforced carbon–carbon studies. His study looks at the relationship between Reactivity and topics such as Photochemistry, which overlap with Ruthenium and Redox.
Michel Pfeffer focuses on Stereochemistry, Ligand, Medicinal chemistry, Catalysis and Ruthenium. His study in Stereochemistry is interdisciplinary in nature, drawing from both Denticity, Metal, Palladium, Cationic polymerization and Stereoselectivity. His research in Ligand tackles topics such as Rhodium which are related to areas like Iridium and Imine.
His Medicinal chemistry study frequently draws parallels with other fields, such as Ring. His Catalysis study necessitates a more in-depth grasp of Organic chemistry. In general Ruthenium study, his work on Osmium often relates to the realm of X-ray crystallography, thereby connecting several areas of interest.
Michel Pfeffer mainly investigates Catalysis, Stereochemistry, Ruthenium, Organic chemistry and Photochemistry. His is doing research in Organic synthesis, Oxidative addition, Transmetalation and Palladium, both of which are found in Catalysis. His Stereochemistry research is multidisciplinary, incorporating elements of Cathepsin B, Enzyme, Ligand and Adamantane.
His biological study spans a wide range of topics, including Molecule, Lipophilicity and In vitro, Structure–activity relationship. Michel Pfeffer integrates many fields in his works, including Organic chemistry and Tandem. His Photochemistry study integrates concerns from other disciplines, such as Medicinal chemistry, Hydride, Ruthenium chloride and Coupling.
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Ru-, Rh-, and Pd-Catalyzed C-C Bond Formation Involving C-H Activation and Addition on Unsaturated Substrates: Reactions and Mechanistic Aspects
Vincent Ritleng;Claude Sirlin;Michel Pfeffer.
Chemical Reviews (2002)
Reactions of cyclopalladated compounds and alkynes: New pathways for organic synthesis?
Recueil des Travaux Chimiques des Pays-Bas (1990)
Cycloruthenated Compounds – Synthesis and Applications
Jean‐Pierre Djukic;Jean‐Baptiste Sortais;Laurent Barloy;Michel Pfeffer.
European Journal of Inorganic Chemistry (2009)
Selected applications to organic synthesis of intramolecular C-H activation reactions by transition metals
Pure and Applied Chemistry (1992)
A Ruthenium-Containing Organometallic Compound Reduces Tumor Growth through Induction of the Endoplasmic Reticulum Stress Gene CHOP
Xiangjun Meng;Mili L. Leyva;Marjorie Jenny;Isabelle Gross.
Cancer Research (2009)
An Effective Route to Cycloruthenated N-Ligands under Mild Conditions
Susana Fernandez;Michel Pfeffer;and Vincent Ritleng;Claude Sirlin.
Ruthenium (II)-Derived Organometallic Compounds Induce Cytostatic and Cytotoxic Effects on Mammalian Cancer Cell Lines through p53-Dependent and p53-Independent Mechanisms
Christian Gaiddon;Pierre Jeannequin;Pierre Bischoff;Michel Pfeffer.
Journal of Pharmacology and Experimental Therapeutics (2005)
Insertion of alkynes into the palladium-carbon bond of palladacycles. Mechanistic information from high-pressure kinetic and x-ray structural data
A. D. Ryabov;Rudi Van Eldik;Guy Le Borgne;Michel Pfeffer.
Reaction of cyclopalladated compounds. 15. Controlled synthesis of heterocyclic compounds through ring enlargement by alkyne insertions into the palladium-carbon bonds of cyclopalladated amines followed by ring closure
Fida. Maassarani;Michel. Pfeffer;Guy. Le Borgne.
New synthesis and new bio-application of cyclometalated ruthenium(II) complexes for fast mediated electron transfer with peroxidase and glucose oxidase.
Alexander D. Ryabov;Valentin S. Sukharev;Larissa Alexandrova;and Ronan Le Lagadec.
Inorganic Chemistry (2001)
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