Fernando J. Lahoz spends much of his time researching Stereochemistry, Medicinal chemistry, Rhodium, Iridium and Catalysis. His studies deal with areas such as Osmium, Ruthenium, Ligand, Crystal structure and Molecule as well as Stereochemistry. His work carried out in the field of Medicinal chemistry brings together such families of science as Alkyne, Hydride and Reactivity, Organic chemistry.
His research in Rhodium intersects with topics in Cationic polymerization, Carbonylation, Regioselectivity and Enantioselective synthesis. His Iridium research includes themes of Photochemistry and Metal. His work deals with themes such as Diels alder and Optically active, which intersect with Catalysis.
Fernando J. Lahoz focuses on Stereochemistry, Medicinal chemistry, Rhodium, Crystal structure and Ligand. His Stereochemistry research is multidisciplinary, relying on both Oxidative addition, Cationic polymerization, Molecule and Ruthenium. Fernando J. Lahoz combines subjects such as Reactivity, Iridium, Organic chemistry and Catalysis with his study of Medicinal chemistry.
His biological study spans a wide range of topics, including Inorganic chemistry, Polymer chemistry, Metal, Carbene and Bicyclic molecule. His research integrates issues of X-ray crystallography, Inorganic compound and Cluster in his study of Crystal structure. His Crystallography research incorporates themes from X-ray and Nuclear magnetic resonance spectroscopy.
Fernando J. Lahoz mostly deals with Medicinal chemistry, Ligand, Catalysis, Stereochemistry and Rhodium. His Medicinal chemistry research includes elements of Cationic polymerization, Reactivity, Iridium and Metal. The concepts of his Ligand study are interwoven with issues in Metallacycle, Proton NMR, Molecule and Crystal structure.
Catalysis is a subfield of Organic chemistry that he tackles. The study incorporates disciplines such as Oxidative addition, Diphosphane and Heterolysis in addition to Stereochemistry. His study in Rhodium is interdisciplinary in nature, drawing from both Stereocenter, Stoichiometry, Electron pair, Frustrated Lewis pair and Reaction mechanism.
His primary areas of investigation include Medicinal chemistry, Catalysis, Ligand, Stereochemistry and Iridium. The Medicinal chemistry study combines topics in areas such as Photochemistry, Molecule, Moiety and Carbene. Fernando J. Lahoz has included themes like Reactivity and Brønsted–Lowry acid–base theory in his Ligand study.
His Stereochemistry research integrates issues from Oxidative addition, Cationic polymerization and Deprotonation. His Iridium research is multidisciplinary, relying on both Selectivity and Metal. Fernando J. Lahoz combines subjects such as Silyl ether, Enantiomer and Reaction mechanism with his study of Rhodium.
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Synthesis, reactivity, molecular structure, and catalytic activity of the novel dichlorodihydridoosmium(IV) complexes OsH2Cl2(Pr3)2 (Pr3 = P-i-Pr3, PMe-t-Bu2)
M. Aracama;M. A. Esteruelas;F. J. Lahoz;J. A. Lopez.
Inorganic Chemistry (1991)
Dopant distribution in a Tm3+–Yb3+ codoped silica based glass ceramic: An infrared-laser induced upconversion study
F. Lahoz;I. R. Martı́n;J. Méndez-Ramos;P. Núñez.
Journal of Chemical Physics (2004)
Rhodium(I) Complexes with Hemilabile N-Heterocyclic Carbenes: Efficient Alkyne Hydrosilylation Catalysts
M. Victoria Jiménez;Jesús J. Pérez-Torrente;M. Isabel Bartolomé;Verena Gierz.
Organometallics (2008)
Ligand-controlled regioselectivity in the hydrothiolation of alkynes by rhodium N-heterocyclic carbene catalysts.
Andrea Di Giuseppe;Ricardo Castarlenas;Jesús J. Pérez-Torrente;Marcello Crucianelli.
Journal of the American Chemical Society (2012)
Five-Coordinate Complex [RuHCl(CO)(PPri3)2] as a Precursor for the Preparation of New Cyclopentadienylruthenium Compounds Containing Unsaturated η1-Carbon Ligands†
Miguel A. Esteruelas;Angel V. Gómez;Fernando J. Lahoz;Ana M. López.
Organometallics (1996)
Iridium(I) Complexes with Hemilabile N-Heterocyclic Carbenes: Efficient and Versatile Transfer Hydrogenation Catalysts
M. Victoria Jiménez;Javier Fernández-Tornos;Jesús J. Pérez-Torrente;Francisco J. Modrego.
Organometallics (2011)
Synthesis of new hydride-carbyne and hydride-vinylcarbyne complexes of osmium(II) by reaction of OsH2Cl2(P-iso-Pr3)2 with terminal alkynes
Jesus Espuelas;Miguel A. Esteruelas;Fernando J. Lahoz;Luis A. Oro.
Journal of the American Chemical Society (1993)
Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to Methacrolein Catalyzed by (η5-C5Me5)M{(R)-Prophos} Containing Complexes (M = Rh, Ir; (R)-Prophos = 1,2-bis(Diphenylphosphino)propane): On the Origin of the Enantioselectivity
Daniel Carmona;M. Pilar Lamata;Fernando Viguri;Ricardo Rodriguez.
Journal of the American Chemical Society (2005)
Reactions of the Dihydrogen Complex OsCl2(.eta.2-H2)(CO)(PiPr3)2 with Terminal Alkynes: Synthesis of Carbene, Vinylcarbene, and .mu.-Bis-carbene Osmium (II) Derivatives
Miguel A. Esteruelas;Fernando J. Lahoz;Enrique Onate;Luis A. Oro.
Journal of the American Chemical Society (1995)
Trimerisation of the Cationic Fragments [(η-ring)M(Aa)]+ ((η-ring) M=(η5-C5Me5)Rh, (η5-C5Me5)Ir, (η6-p-MeC6H4iPr)Ru; Aa=α-amino acidate) with Chiral Self-Recognition: Synthesis, Characterisation, Solution Studies and Catalytic Reactions of the Trimers [{(η-ring)M(Aa)}3](BF4)3
Daniel Carmona;Fernando J. Lahoz;Reinaldo Atencio;Luis A. Oro.
Chemistry: A European Journal (1999)
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