Paul Müller focuses on Catalysis, Medicinal chemistry, Rhodium, Organic chemistry and Stereochemistry. His study in Cyclopropanation, Nitrene, Allylic rearrangement, Olefin fiber and Stereospecificity is carried out as part of his Catalysis studies. His Nitrene study combines topics from a wide range of disciplines, such as Reagent, Walden inversion and Intermolecular force.
His Medicinal chemistry research is multidisciplinary, relying on both Yield, Enantioselective synthesis, Carboxylate, Intramolecular force and Carbenoid. In his study, which falls under the umbrella issue of Rhodium, Kinetic resolution, Steric effects and Reactivity is strongly linked to Amination. The Stereochemistry study combines topics in areas such as Cyclopropene and Homogeneous catalysis.
Medicinal chemistry, Organic chemistry, Catalysis, Stereochemistry and Enantioselective synthesis are his primary areas of study. His Medicinal chemistry study integrates concerns from other disciplines, such as Photochemistry, Intramolecular force, Carbenoid and Carbene. His study explores the link between Intramolecular force and topics such as Diazo that cross with problems in Asymmetric induction.
Allylic rearrangement is closely connected to Yield in his research, which is encompassed under the umbrella topic of Catalysis. His Stereochemistry research integrates issues from Solvolysis, Reaction rate and Stereospecificity. His Rhodium research is multidisciplinary, incorporating perspectives in Amination and Carboxylate.
His primary areas of study are Catalysis, Medicinal chemistry, Organic chemistry, Enantioselective synthesis and Cyclopropanation. He combines subjects such as Decomposition and Intramolecular force with his study of Catalysis. His research in Medicinal chemistry is mostly focused on Diazo.
In general Organic chemistry study, his work on Cyclopropane, Ruthenium, Sulfonyl and Steric effects often relates to the realm of Amino acid, thereby connecting several areas of interest. His Enantioselective synthesis research incorporates elements of Enol, Stereochemistry and Cycloaddition. His research in Cyclopropanation intersects with topics in Olefin fiber, Transition metal, Carbene, Selectivity and Ylide.
His scientific interests lie mostly in Catalysis, Medicinal chemistry, Organic chemistry, Rhodium and Cyclopropanation. His Catalysis research incorporates themes from Carboxylate and Stereochemistry. His Medicinal chemistry research is multidisciplinary, relying on both Intramolecular force and Allylic rearrangement.
His Cyclopropanation research is multidisciplinary, incorporating elements of Diazo, Carbenoid and Ylide. Paul Müller focuses mostly in the field of Diazo, narrowing it down to matters related to Selectivity and, in some cases, Enol and Photochemistry. His Nitrene study combines topics in areas such as Amination and Intermolecular force.
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Enantioselective catalytic aziridinations and asymmetric nitrene insertions into CH bonds.
Paul Müller;Corinne Fruit.
Chemical Reviews (2003)
Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)
P. Muller.
Pure and Applied Chemistry (1994)
Efficient diastereoselective intermolecular rhodium-catalyzed C-H amination.
Chungen Liang;Fabien Robert-Peillard;Corinne Fruit;Paul Müller.
Angewandte Chemie (2006)
Rhodium(II)-Catalyzed CH Insertions with {[(4-Nitrophenyl)sulfonyl]imino}phenyl-λ3-iodane
Ivo Nageli;Corine Baud;Gérald Hugues Bernardinelli;Yvan Daniel Michel Jacquier.
Helvetica Chimica Acta (1997)
High enantioselectivity in the intramolecular cyclopropanation of allyl diazoacetates using a novel rhodium(II) catalyst
Michael P. Doyle;Roland J. Pieters;Stephen F. Martin;Richard E. Austin.
Journal of the American Chemical Society (1991)
A method for rhodium(II)-catalyzed aziridination of olefins
Paul Müller;Corine Baud;Yvan Jacquier.
Tetrahedron (1996)
Asymmetric transfer of carbenes with phenyliodonium ylides.
Paul Müller.
Accounts of Chemical Research (2004)
Catalyzed oxidation of alcohols and aldehydes with iodosylbenzene
Paul Müller;José Godoy.
Tetrahedron Letters (1981)
Effective Uses of Dirhodium(II) Tetrakis[methyl 2-oxopyrrolidine-5(R or S)-carboxylate] for Highly Enantioselective Intermolecular Cyclopropenation Reactions
Michael P. Doyle;Marina Protopopova;Paul Muller;Doina Ene.
Journal of the American Chemical Society (1994)
Rhodium(II)-catalyzed olefin cyclopropanation with the phenyliodonium ylide derived from Meldrum's acid
Paul Müller;Yves Allenbach;Estelle Robert.
Tetrahedron-asymmetry (2003)
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