His primary areas of study are Stereochemistry, Catalysis, Organic chemistry, Aldol reaction and Aldolase A. His Stereochemistry research incorporates elements of Crystallography, Ligand, Molecule, Aqueous solution and Reaction mechanism. His Ligand research is multidisciplinary, relying on both Ethylamine, Ruthenium, Two-dimensional nuclear magnetic resonance spectroscopy, Photochemistry and Pyrazole.
His research integrates issues of Dihydroxyacetone phosphate and Stereoselectivity in his study of Aldol reaction. Teodor Parella has included themes like Biocatalysis, Enzyme catalysis, Organic synthesis, Dihydroxyacetone and Glycolaldehyde in his Aldolase A study. In Heteronuclear molecule, Teodor Parella works on issues like Chemical physics, which are connected to Nuclear magnetic resonance.
Teodor Parella mostly deals with Stereochemistry, Analytical chemistry, Organic chemistry, Catalysis and Nuclear magnetic resonance spectroscopy. His Stereochemistry research includes themes of Aldol reaction, Cycloaddition, Crystallography, Ligand and Aldolase A. His Ligand research focuses on Ruthenium and how it connects with Photochemistry and Ethylamine.
He has researched Analytical chemistry in several fields, including Heteronuclear molecule, Pulse sequence and Heteronuclear single quantum coherence spectroscopy. The concepts of his Heteronuclear molecule study are interwoven with issues in Spin states and Homonuclear molecule. His studies in Catalysis integrate themes in fields like Combinatorial chemistry, Intramolecular force, Medicinal chemistry and Polymer chemistry.
Teodor Parella mainly focuses on Stereochemistry, Catalysis, Nuclear magnetic resonance spectroscopy, Heteronuclear molecule and Coupling constant. His Stereochemistry research is multidisciplinary, incorporating elements of Nucleophile and Aldolase A. His Catalysis study combines topics from a wide range of disciplines, such as Combinatorial chemistry, Aryl, Ligand and Medicinal chemistry.
His work investigates the relationship between Nuclear magnetic resonance spectroscopy and topics such as Dipole that intersect with problems in Isotropy and Anisotropy. He combines subjects such as Homonuclear molecule and NMR spectra database with his study of Heteronuclear molecule. His work in Analytical chemistry tackles topics such as Heteronuclear single quantum coherence spectroscopy which are related to areas like Molecular physics.
Teodor Parella mainly investigates Analytical chemistry, Coupling constant, Nuclear magnetic resonance spectroscopy, Catalysis and Nuclear magnetic resonance. His Analytical chemistry research integrates issues from Chemical physics, Heteronuclear single quantum coherence spectroscopy, Chromatography, Molecule and Small molecule. Within one scientific family, Teodor Parella focuses on topics pertaining to Dipole under Nuclear magnetic resonance spectroscopy, and may sometimes address concerns connected to Physical chemistry, In situ and Stereocenter.
His work deals with themes such as Combinatorial chemistry, Aryl, Reactivity and Cationic polymerization, which intersect with Catalysis. His work in the fields of Nuclear magnetic resonance, such as Heteronuclear molecule and J resolved, overlaps with other areas such as Transformation. His Intramolecular force study is concerned with Stereochemistry in general.
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A new Ru complex capable of catalytically oxidizing water to molecular dioxygen
Cristina Sens;Isabel Romero;Montserrat Rodríguez;Antoni Llobet.
Journal of the American Chemical Society (2004)
Direct observation of CuI/CuIII redox steps relevant to Ullmann-type coupling reactions
Alicia Casitas;Amanda E. King;Teodor Parella;Miquel Costas.
Chemical Science (2010)
Anti-inflammatory and analgesic activity of Baccharis trimera: identification of its active constituents.
Rosa M. Gené;Carme Cartañá;Tomás Adzet;Esther Marín.
Planta Medica (1996)
Aryl CH Activation by CuII To Form an Organometallic Aryl–CuIII Species: A Novel Twist on Copper Disproportionation†
Xavi Ribas;Deanne A. Jackson;Bruno Donnadieu;José Mahía.
Angewandte Chemie (2002)
PULSED FIELD GRADIENTS : A NEW TOOL FOR ROUTINE NMR
Magnetic Resonance in Chemistry (1998)
Fructose-6-phosphate aldolase in organic synthesis: preparation of D-fagomine, N-alkylated derivatives, and preliminary biological assays
José A. Castillo;Jordi Calveras;Josefina Casas;Montserrat Mitjans.
Organic Letters (2006)
Opposite metabolic responses of shoots and roots to drought.
Albert Gargallo-Garriga;Jordi Sardans;Míriam Pérez-Trujillo;Albert Rivas-Ubach.
Scientific Reports (2015)
Broadband 1H homodecoupled NMR experiments: recent developments, methods and applications
Laura Castañar;Teodor Parella.
Magnetic Resonance in Chemistry (2015)
Facile C―H Bond Cleavage via a Proton-Coupled Electron Transfer Involving a C―H···CuII Interaction
Xavi Ribas;Carlos Calle;Albert Poater;Alicia Casitas.
Journal of the American Chemical Society (2010)
Asymmetric Self‐ and Cross‐Aldol Reactions of Glycolaldehyde Catalyzed by D‐Fructose‐6‐phosphate Aldolase
Xavier Garrabou;José A. Castillo;Christine Guérard-Hélaine;Teodor Parella.
Angewandte Chemie (2009)
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