His primary areas of investigation include Organic chemistry, Medicinal chemistry, Stereochemistry, Catalysis and Aryl. Reagent, Intramolecular force, Reactivity, Ketone and Pyridine are subfields of Organic chemistry in which his conducts study. His work carried out in the field of Medicinal chemistry brings together such families of science as Transition metal carbene complex, Carbene, Halogenation and Annulation.
His work deals with themes such as Amino acid, Phenylalanine, Enamine and Reaction mechanism, which intersect with Stereochemistry. His studies deal with areas such as Mercury and Chloride as well as Catalysis. His Aryl research is multidisciplinary, incorporating perspectives in Halide, Polymer chemistry, Coupling reaction and Imine.
The scientist’s investigation covers issues in Organic chemistry, Medicinal chemistry, Aliphatic compound, Stereochemistry and Transition metal carbene complex. His studies in Reagent, Lithium, Reactivity, One-pot synthesis and Stereoselectivity are all subfields of Organic chemistry research. José Barluenga interconnects Aryl, Electrophile and Regioselectivity in the investigation of issues within Medicinal chemistry.
His Aliphatic compound study integrates concerns from other disciplines, such as Ketone, Nuclear magnetic resonance spectroscopy and Aldehyde. His Transition metal carbene complex study improves the overall literature in Carbene. His study in Carbene is interdisciplinary in nature, drawing from both Chromium, Cycloaddition and Annulation.
José Barluenga mostly deals with Organic chemistry, Carbene, Transition metal carbene complex, Stereochemistry and Medicinal chemistry. His study in Catalysis, Reactivity, Ligand, Enantiopure drug and Coupling reaction falls under the purview of Organic chemistry. The study incorporates disciplines such as Chromium, Group, Alkoxy group and Cycloaddition in addition to Carbene.
The concepts of his Transition metal carbene complex study are interwoven with issues in Hydride, Rhodium, Moiety, Polymer chemistry and Cyclopropanation. José Barluenga has included themes like Reaction mechanism, Alkyne, Ring and Stereoselectivity in his Stereochemistry study. While the research belongs to areas of Medicinal chemistry, he spends his time largely on the problem of Annulation, intersecting his research to questions surrounding Regioselectivity.
José Barluenga focuses on Organic chemistry, Medicinal chemistry, Catalysis, Stereochemistry and Palladium. His study in Coupling reaction, Pyridine, Reactivity, Reagent and Regioselectivity is done as part of Organic chemistry. His Medicinal chemistry study combines topics from a wide range of disciplines, such as Aryl and Annulation.
In Catalysis, José Barluenga works on issues like Intramolecular force, which are connected to Combinatorial chemistry and Bicyclic molecule. The various areas that José Barluenga examines in his Stereochemistry study include Phenylalanine, Carbene, Alkyl and Reaction mechanism. In his work, Azide, Triazole, Sodium azide and Imine is strongly intertwined with Amination, which is a subfield of Palladium.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Metal-free carbon–carbon bond-forming reductive coupling between boronic acids and tosylhydrazones
José Barluenga;María Tomás-Gamasa;Fernando Aznar;Carlos Valdés.
Nature Chemistry (2009)
Modern Heterocyclic Chemistry: BARLUENGA:HETEROCYC. 4VOL O-BK
Julio Alvarez-Builla;Juan Jose Vaquero;José Barluenga.
(2011)
Modern heterocyclic chemistry
Julio Alvarez-Builla;Juan Jose Vaquero;José Barluenga.
(2011)
I(py)2BF4, a New Reagent in Organic Synthesis: General Method for the 1,2‐Iodofunctionalization of Olefins
José Barluenga;José M. González;Pedro J. Campos;Gregorio Asensio.
Angewandte Chemie (1985)
Developments in Pd Catalysis: Synthesis of 1H‐1,2,3‐Triazoles from Sodium Azide and Alkenyl Bromides
José Barluenga;Carlos Valdés;Gustavo Beltrán;María Escribano.
Angewandte Chemie (2006)
High Diastereoselective Synthesis of Threo or Erythro Aminoalkyl Epoxides from .alpha.-Amino Acids
Jose Barluenga;Beatriz Baragana;Jose M. Concellon.
Journal of Organic Chemistry (1995)
Tosylhydrazone – neue Anwendungen klassischer Reagentien in palladiumkatalysierten Kreuzkupplungen und metallfreien Umsetzungen
José Barluenga;Carlos Valdés.
Angewandte Chemie (2011)
Intramolecular diamination of alkenes with palladium(II)/copper(II) bromide and IPy2BF4: the role of halogenated intermediates.
Kilian Muñiz;Claas H. Hövelmann;Esther Campos-Gómez;José Barluenga.
Chemistry-an Asian Journal (2008)
Transferring iodine: more than a simple functional group exchange in organic synthesis
José Barluenga.
Pure and Applied Chemistry (1999)
Arylation of α-Chiral Ketones by Palladium-Catalyzed Cross-Coupling Reactions of Tosylhydrazones with Aryl Halides
José Barluenga;María Escribano;Fernando Aznar;Carlos Valdés.
Angewandte Chemie (2010)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Alicante
University of Oviedo
University of Valencia
University of Oviedo
University of Alicante
Max Planck Society
Institució Catalana de Recerca i Estudis Avançats
Instituto de Biologia Molecular e Celular
Universidade Nova de Lisboa
University of Helsinki
Princeton University
University of Washington
Chinese Academy of Sciences
University of New South Wales
Grenoble Alpes University
University of Delaware
Grenoble Alpes University
Stanford University
Max Planck Society
Friedrich-Loeffler-Institut
Cornell University
University of Oslo
Mayo Clinic
University of Auckland
Max Planck Society
Harvard University