His scientific interests lie mostly in Stereochemistry, Crystal structure, Lithium, Medicinal chemistry and Crystallography. His work carried out in the field of Stereochemistry brings together such families of science as Bond length and Benzoxazole. His biological study spans a wide range of topics, including Physical chemistry, Molecule, Redox, Diamine and Dichloromethane.
His Lithium study incorporates themes from Solid state structure and n-Butyllithium. His research in the fields of Tetramethylethylenediamine overlaps with other disciplines such as Structure analysis. His studies in Crystallography integrate themes in fields like Carbanion and Diethyl ether.
His main research concerns Crystal structure, Medicinal chemistry, Crystallography, Stereochemistry and Molecule. The concepts of his Crystal structure study are interwoven with issues in Inorganic compound, Diamine, Polymer chemistry and Lithium. His Polymer chemistry research includes themes of Photochemistry and Amine gas treating.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Tertiary amine, Diethyl ether and Sulfone. In the subject of general Crystallography, his work in Tetrahedron is often linked to X-ray, thereby combining diverse domains of study. Michael Marsch has researched Stereochemistry in several fields, including Tetrahydrofuran and Ring.
His primary scientific interests are in Medicinal chemistry, Stereochemistry, Ring, Crystal structure and Catalysis. His Medicinal chemistry research focuses on Crystal and how it connects with Hydrogen bond. His work in the fields of Absolute configuration, Epimer and Moiety overlaps with other areas such as Dipeptide and Cysteine.
His research integrates issues of Dihedral angle, Thio-, Molecule and Thiophene in his study of Crystal structure. He has included themes like Radical and Chirality in his Catalysis study. He focuses mostly in the field of Radical, narrowing it down to matters related to Photochemistry and, in some cases, Radical ion.
His scientific interests lie mostly in Catalysis, Enantioselective synthesis, Stereochemistry, Photoredox catalysis and Radical. His research in Catalysis intersects with topics in Chirality and Medicinal chemistry. His Chirality study combines topics in areas such as Octahedron, Ruthenium, Polymer chemistry, Metal and Trifluoromethyl.
Stereochemistry is closely attributed to Stereoselectivity in his work. The Radical study combines topics in areas such as Rhodium, Organocatalysis, Photochemistry, Catalytic cycle and Asymmetric induction. His Photochemistry research incorporates elements of Amination and Chiral Lewis acid.
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.
Asymmetric photoredox transition-metal catalysis activated by visible light
Haohua Huo;Xiaodong Shen;Chuanyong Wang;Lilu Zhang.
Nature (2014)
The Crystal Structures of a Lower Order and a “Higher Order” Cyanocuprate: [tBuCu(CN)Li(OEt2)2]∞ and [tBuCutBu{Li(thf)(pmdeta)}2CN]
Gernot Boche;Ferdinand Bosold;Michael Marsch;Klaus Harms.
Angewandte Chemie (1998)
η1-C6H5CH2Li•THF•TMEDA, Kristallstruktur eines Benzyllithium•THF•TMEDA-Komplexes mit einem pyramidalen Benzyl-C-Atom
Wolfgang Zarges;Michael Marsch;Klaus Harms;Gernot Boche.
Chemische Berichte (1989)
Generation of Enantiomerically Enriched Lithium Indenides by Means of (–)‐Sparteine: Structure, Stereoselective Substitution, and Solvent Effects
Inga Hoppe;Michael Marsch;Klaus Harms;Gernot Boche.
Angewandte Chemie (1995)
Röntgenstrukturuntersuchung von α‐(Trimethylsilyl)benzyllithium·Tetramethylendiamin [C6H5CH(SiMe3)Li·TMEDA] und α‐(Phenylthio)‐benzyllithium·3 Tetrahydrofuran [C6H5CH(SPh)Li·(THF)3] – zwei zentral‐chirale Benzyllithium‐Verbindungen
Wolfgang Zarges;Michael Marsch;Klaus Harms;Gernot Frenking.
Chemische Berichte (1991)
The relation between ion pair structures and reactivities of lithium cuprates
Michael John;Carsten Auel;Christoph Behrens;Michael Marsch.
Chemistry: A European Journal (2000)
Crystal and electronic structure of stable nitrenium ions. A comparison with structurally related carbenes
Gernot Boche;Phil Andrews;Klaus Harms;Michael Marsch.
Journal of the American Chemical Society (1996)
Octahedral Ruthenium Complex with Exclusive Metal-Centered Chirality for Highly Effective Asymmetric Catalysis
Yu Zheng;Yuqi Tan;Klaus Harms;Michael Marsch.
Journal of the American Chemical Society (2017)
[(α‐Cyanobenzyllithium. Tetramethylethylenediamine)2. Benzene]: X‐ray Structure Analysis of an α‐Nitrile “Carbanion”
G. Boche;M. Marsch;K. Harms.
Angewandte Chemie (1986)
α‐Oxygen‐Substituted Organolithium Compounds and Their Carbenoid Nature: Calculations of the Configurational Stability and of LiCH2OH Model Structures, Crystal Structure of Diphenyl(trimethylsilyloxy)methyllithium · 3 THF, and the Stereochemistry of the (Reverse) Brook Rearrangement
Gernot Boche;Achim Opel;Michael Marsch;Klaus Harms.
Chemische Berichte (1992)
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