His scientific interests lie mostly in Stereochemistry, Catalysis, Enantioselective synthesis, Organic chemistry and Crystal structure. The various areas that Klaus Harms examines in his Stereochemistry study include Molecule, Ligand, Metal and Ruthenium. His Catalysis study integrates concerns from other disciplines, such as Medicinal chemistry and Polymer chemistry.
His Enantioselective synthesis study incorporates themes from Combinatorial chemistry, Photochemistry, Iridium and Chirality. His Crystal structure research is included under the broader classification of Crystallography. His research in Crystallography intersects with topics in Tetramethylethylenediamine, Inorganic chemistry, X-ray crystallography, Copper and Ion.
His primary areas of investigation include Stereochemistry, Crystal structure, Crystallography, Medicinal chemistry and Organic chemistry. His study in Stereochemistry is interdisciplinary in nature, drawing from both Ring and Stereoselectivity. His Crystal structure research integrates issues from X-ray crystallography, Molecule, Polymer chemistry and Lithium.
His Crystallography research is multidisciplinary, incorporating perspectives in Inorganic chemistry, Ligand and Hydrogen bond. His Catalysis and Enantioselective synthesis investigations are all subjects of Organic chemistry research. His Catalysis study combines topics in areas such as Combinatorial chemistry, Photochemistry and Cobalt.
Klaus Harms mostly deals with Catalysis, Stereochemistry, Enantioselective synthesis, Crystallography and Crystal structure. His Catalysis research incorporates elements of Combinatorial chemistry and Photochemistry. His work in Stereochemistry addresses subjects such as Medicinal chemistry, which are connected to disciplines such as Aryl.
His Enantioselective synthesis research focuses on subjects like Chirality, which are linked to Lewis acids and bases. In Crystallography, Klaus Harms works on issues like Copper, which are connected to Coordination polymer. He has researched Crystal structure in several fields, including Luminescence, Molecule and Nanotechnology.
Klaus Harms mainly investigates Catalysis, Enantioselective synthesis, Stereochemistry, Crystallography and Rhodium. His Catalysis study frequently draws parallels with other fields, such as Medicinal chemistry. His biological study spans a wide range of topics, including Photoredox catalysis, Polymer chemistry, Photochemistry, Chirality and Combinatorial chemistry.
Klaus Harms combines subjects such as Denticity, Metal ions in aqueous solution, Metal, Dicyanamide and Hydrogen bond with his study of Stereochemistry. His Crystallography research is multidisciplinary, relying on both Azide and Nickel. His work deals with themes such as Single crystal and Square pyramidal molecular geometry, Ligand, Crystal structure, Copper, which intersect with Schiff base.
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Asymmetric photoredox transition-metal catalysis activated by visible light
Haohua Huo;Xiaodong Shen;Chuanyong Wang;Lilu Zhang.
Nature (2014)
Crystallographic characterization of a synthetic 1:1 end-on copper dioxygen adduct complex.
Christian Würtele;Ekaterina Gaoutchenova;Klaus Harms;Max C. Holthausen.
Angewandte Chemie (2006)
Highly enantioselective intra- and intermolecular [2 + 2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: host-guest interactions, product configuration, and the origin of the stereoselectivity in solution.
Thorsten Bach;Hermann Bergmann;Benjamin Grosch;Klaus Harms.
Journal of the American Chemical Society (2002)
Structurally Sophisticated Octahedral Metal Complexes as Highly Selective Protein Kinase Inhibitors
Li Feng;Yann Geisselbrecht;Sebastian Blanck;Alexander Wilbuer.
Journal of the American Chemical Society (2011)
Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes
Jasna Maksimoska;Li Feng;Klaus Harms;Chunling Yi.
Journal of the American Chemical Society (2008)
Expression of a bacterial serine acetyltransferase in transgenic potato plants leads to increased levels of cysteine and glutathione
K Harms;P von Ballmoos;C Brunold;R Höfgen.
Plant Journal (2000)
Phosphabenzenes as Monodentate π-Acceptor Ligands for Rhodium-Catalyzed Hydroformylation
Bernhard Breit;Roland Winde;Thomas Mackewitz;Rocco Paciello.
Chemistry: A European Journal (2001)
Asymmetric Radical-Radical Cross-Coupling through Visible-Light-Activated Iridium Catalysis.
Chuanyong Wang;Jie Qin;Xiaodong Shen;Radostan Riedel.
Angewandte Chemie (2016)
Crown Ethers with a Lewis Acidic Center: A New Class of Heterotopic Host Molecules
Manfred T. Reetz;Christof M. Niemeyer;Klaus Harms.
Angewandte Chemie (1991)
1,8-Bis(hexamethyltriaminophosphazenyl)naphthalene, HMPN: a superbasic bisphosphazene "proton sponge".
Volker Raab;Ekaterina Gauchenova;Alexei Merkoulov;Klaus Harms.
Journal of the American Chemical Society (2005)
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