Stereochemistry, Crystallography, Medicinal chemistry, Crystal structure and Reactivity are his primary areas of study. His biological study spans a wide range of topics, including Ligand, Sulfur, Deprotonation and Nucleophile. His studies deal with areas such as Inorganic chemistry, Ion, Molecule and Delocalized electron as well as Crystallography.
His Medicinal chemistry research includes themes of Organic chemistry, Ring and Alkyl. His Crystal structure study integrates concerns from other disciplines, such as Samarium, Steric effects, X-ray crystallography, Methylene and Divalent. He has researched Reactivity in several fields, including Pyridine, Pincer movement, Homoleptic, Carbene and Double bond.
His scientific interests lie mostly in Stereochemistry, Crystallography, Crystal structure, Medicinal chemistry and Organic chemistry. His Stereochemistry study also includes fields such as
His Crystal structure research includes elements of Phosphole, Cyclopentadienyl complex, Phosphorus, X-ray crystallography and Nuclear magnetic resonance spectroscopy. His Medicinal chemistry study combines topics in areas such as Yield, Photochemistry, Cationic polymerization and Catalysis. As part of his studies on Organic chemistry, Louis Ricard often connects relevant subjects like Polymer chemistry.
Louis Ricard mainly focuses on Stereochemistry, Crystallography, Medicinal chemistry, Crystal structure and Ligand. Louis Ricard combines subjects such as Chelation, Ferrocene, Enantiopure drug, Reactivity and Stereoselectivity with his study of Stereochemistry. His study focuses on the intersection of Crystallography and fields such as Inorganic chemistry with connections in the field of Phosphorus.
The study incorporates disciplines such as Cationic polymerization, Organic chemistry, Catalysis, Regioselectivity and Aryl in addition to Medicinal chemistry. His Crystal structure research incorporates themes from Phosphonate, Cyclopentadienyl complex, Solvation, Pincer movement and Deprotonation. His Ligand research is multidisciplinary, incorporating elements of Derivative, Yield, Polymer chemistry and Palladium.
Louis Ricard mostly deals with Stereochemistry, Medicinal chemistry, Ligand, Reactivity and Crystallography. His Stereochemistry research incorporates elements of Trifluoromethyl, Oxidative cyclization, Polymer chemistry and Chiral auxiliary. His Medicinal chemistry research is multidisciplinary, relying on both Denticity, Aryl, Alkyl and Phosphine.
His research on Ligand also deals with topics like
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Phosphine gold(I) bis-(trifluoromethanesulfonyl)imidate complexes as new highly efficient and air-stable catalysts for the cycloisomerization of enynes.
Nicolas Mézailles;Louis Ricard;Fabien Gagosz.
Organic Letters (2005)
Asymmetric Synthesis and Highly Diastereoselective ortho-Lithiation of Ferrocenyl Sulfoxides. Application to the Synthesis of Ferrocenyl Derivatives with Planar Chirality
François Rebière;Olivier Riant;Louis Ricard;Henri B. Kagan.
Angewandte Chemie (1993)
An Ni4 Single‐Molecule Magnet: Synthesis, Structure and Low‐Temperature Magnetic Behavior
María Moragues-Cánovas;Madeleine Helliwell;Louis Ricard;Éric Rivière.
European Journal of Inorganic Chemistry (2004)
Complexes of functional phosphines. 4. Coordination properties of (diphenylphosphino)acetonitrile, ethyl (diphenylphosphino)acetate and corresponding carbanions. Characterization of a new facile reversible carbon dioxide insertion into palladium(II) complexes
Pierre Braunstein;Dominique Matt;Yves Dusausoy;Jean Fischer.
Journal of the American Chemical Society (1981)
A general route to enantiomerically pure sulfoxides from a chiral sulfite
F. Rebiere;O. Samuel;L. Ricard;H. B. Kagan.
Journal of Organic Chemistry (1991)
The structure of the heteropolytungstate (NH4)17Na NaW21Sb9O86-14H2O. An inorganic crypate.
Jean Fischer;Louis Ricard;Raymond Weiss.
Journal of the American Chemical Society (1976)
New mono- and bis-carbene samarium complexes: synthesis, X-ray crystal structures and reactivity.
Thibault Cantat;Florian Jaroschik;François Nief;Louis Ricard.
Chemical Communications (2005)
Mechanism of the Stille reaction catalyzed by palladium ligated to arsine ligand: PhPdI(AsPh3)(DMF) is the species reacting with vinylstannane in DMF.
Christian Amatore;Ali A. Bahsoun;Anny Jutand;Gilbert Meyer.
Journal of the American Chemical Society (2003)
BIPNOR: A New, Efficient Bisphosphine Having Two Chiral, Nonracemizable, Bridgehead Phosphorus Centers for Use in Asymmetric Catalysis
Frédéric Robin;François Mercier;Louis Ricard;François Mathey.
Chemistry: A European Journal (1997)
Silacalix-[n]-phosphaarenes: Macrocyclic Ligands Based on Dicoordinate Phosphorus Centers
Narcis Avarvari;Nicolas Mézailles;Louis Ricard;Pascal Le Floch.
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