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Angewandte Chemie International Edition, ISSN 1433-7851, 12/2013, Volume 52, Issue 52, pp. 14131 - 14134
Ironing out hydrogenation: For the first time, an iron catalyst provided chemo‐ and stereo‐selective semi‐hydrogenation of alkynes to E... 
homogeneous catalysis | stereoselectivity | iron pincer complex | hydrogenation | alkynes | ASYMMETRIC TRANSFER HYDROGENATION | MECHANISM | HYDROSILYLATION | TRANS | CHEMISTRY, MULTIDISCIPLINARY | MILD | KETONES | REDUCTION | LIGAND | Hydrogenation | Iron | Catalysts | Drawing and ironing | Tolerances | Functional groups | Alkynes
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2018, Volume 24, Issue 19, pp. 4780 - 4784
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2018, Volume 140, Issue 8, pp. 3156 - 3169
The hydrogenation of internal alkynes with [Cp*Ru]-based catalysts is distinguished by an unorthodox stereochemical course in that E-alkenes are formed by trans-delivery of the two H atoms of H2... 
E-SELECTIVE SEMIHYDROGENATION | LITHIUM ALUMINUM-HYDRIDE | CATALYTIC-HYDROGENATION | PROPARGYLIC ALCOHOLS | PARAHYDROGEN-INDUCED POLARIZATION | STEREOSPECIFIC SYNTHESIS | STEREOSELECTIVE HYDROGENATION | REDOX ISOMERIZATION | DIRHODIUM CARBENE | CHEMISTRY, MULTIDISCIPLINARY | METATHESIS CATALYST | Molecules | Ruthenium | Olefins | Analysis | Isomerization | Oxidation-reduction reaction | Chemical properties | Research | Hydrogenation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2014, Volume 53, Issue 45, pp. 12210 - 12213
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 14, pp. 3552 - 3557
The metal‐free activation of hydrogen by frustrated Lewis pairs (FLPs) is a valuable method for the hydrogenation of polarized unsaturated molecules ranging from imines, enamines, and silyl enol ethers to heterocycles... 
boranes | metathesis | hydrogenation | olefins | frustrated Lewis pairs | HETEROLYTIC DIHYDROGEN ACTIVATION | FACILE ACTIVATION | FREE CATALYTIC-HYDROGENATION | H-2 ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | CLUSTER-FREE HYDROGENASE | HOMOGENEOUS HYDROGENATION | H2 ACTIVATION | ASYMMETRIC HYDROGENATION | CARBON-DIOXIDE | Boranes - chemistry | Hydrocarbons | Models, Molecular | Molecular Structure | Catalysis | Hydrogen - chemistry | Hydrogenation | Hydrogen | Hydrogen storage | Imines | Unsaturated | Transformations | Ethers | Conversion
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2019, Volume 58, Issue 22, pp. 7329 - 7334
An efficient nickel‐catalyzed asymmetric hydrogenation of N‐tBu‐sulfonyl imines was developed with excellent yields and enantioselectivities using (R,R)‐QuinoxP* as a chiral ligand... 
amines | reaction mechanisms | nickel | asymmetric catalysis | hydrogenation | ALKENE HYDROGENATION | COMPLEXES | IRON | CHEMISTRY, MULTIDISCIPLINARY | KETONES | LIGANDS | ENANTIOSELECTIVE HYDROGENATION | HYDROCHLORIDES | METAL | REDUCTIVE AMINATION | COBALT | Schiff bases | Nickel | Catalysis | Hydrogenation | Asymmetry | Imines | Catalysts | Catalytic activity | Enantiomers | Substrates
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2016, Volume 55, Issue 47, pp. 14653 - 14657
Journal Article