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1. Full Text Pincer‐Type Complexes for Catalytic (De)Hydrogenation and Transfer (De)Hydrogenation Reactions: Recent Progress
by Werkmeister, Svenja and Neumann, Jacob and Junge, Kathrin and Beller, Matthias
Chemistry – A European Journal, ISSN 0947-6539, 08/2015, Volume 21, Issue 35, pp. 12226 - 12250
Pincer complexes are becoming increasingly important for organometallic chemistry and organic synthesis. Since numerous applications for such catalysts have... 
transfer hydrogenation | dehydrogenation | homogeneous catalysis | hydrogenation | pincer complexes | NOZAKI-HIYAMA ALLYLATION | BASE-FREE CONDITIONS | BIS(OXAZOLINYL)PHENYLRHODIUM(III) AQUA COMPLEXES | OXYGEN-ATOM SOURCE | METAL-LIGAND COOPERATION | CHEMISTRY, MULTIDISCIPLINARY | TRANSFER HYDROGENATION REACTIONS | HIGHLY-ACTIVE CATALYSTS | EFFICIENT HYDROGENATION | C-H BORYLATION | OXIDANT-FREE CONVERSION | Dehydrogenation | Hydrogenation | Catalysis | Ruthenium | Catalysts | Metalorganic compounds | Transformations | Iron | Bonding
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2. Full Text Unprecedented Iron‐Catalyzed Ester Hydrogenation. Mild, Selective, and Efficient Hydrogenation of Trifluoroacetic Esters to Alcohols Catalyzed by an Iron Pincer Complex
by Zell, Thomas and Ben‐David, Yehoshoa and Milstein, David
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 18, pp. 4685 - 4689
The synthetically important, environmentally benign hydrogenation of esters to alcohols has been accomplished in recent years only with precious‐metal‐based... 
homogenous catalysis | pincer ligands | esters | hydrogenation | iron complexes | SUBSTRATE SCOPE | ASYMMETRIC TRANSFER HYDROGENATION | HYDROSILYLATION | RUTHENIUM | METAL-LIGAND COOPERATION | ALDEHYDES | AROMATIZATION-DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | REDUCTION | BOND ACTIVATION | CARBON-DIOXIDE | Esters | Hydrogenation | Iron | Iron and steel industry | Catalysts | Catalysis | Trifluoroacetates | Alcohols
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3. Homogeneous hydrogenation
by James, Brian R
1973, ISBN 0471439150, xiv, 525
Hydrogenation | Catalysis
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4. The handbook of homogeneous hydrogenation
by Vries, Johannes G. de and Elsevier, Cornelis J
2007, ISBN 9783527311613, 3 v. (xxxii, 1568 p.)
Catalysts | Hydrogenation | Catalysis
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5. Full Text Transfer Hydrogenation and Hydrogenation of Commercial‐Grade Aldehydes to Primary Alcohols Catalyzed by 2‐(Aminomethyl)pyridine and Pincer Benzo[h]quinoline Ruthenium Complexes
by Baldino, Salvatore and Facchetti, Sarah and Zanotti‐Gerosa, Antonio and Nedden, Hans Günter and Baratta, Walter
ChemCatChem, ISSN 1867-3880, 07/2016, Volume 8, Issue 13, pp. 2279 - 2288
The chemoselective reduction of commercial‐grade aldehydes (97–99 %) to primary alcohols is achieved with cis‐[RuCl2(ampy)(PP)] [ampy=2‐(aminomethyl)pyridine;... 
ruthenium | aldehydes | alcohols | hydrogen transfer | hydrogenation | TRANSFER REDUCTION | ASYMMETRIC TRANSFER HYDROGENATION | CHEMISTRY, PHYSICAL | CARBONYL-COMPOUNDS | HYDRIDE COMPLEXES | HIGHLY EFFICIENT | TISHCHENKO REACTION | HOMOGENEOUS HYDROGENATION | CHEMOSELECTIVE TRANSFER HYDROGENATION | SELECTIVE HYDROGENATION | MEERWEIN-PONNDORF-VERLEY | Alkaloids | Pyridine | Ruthenium | Hydrogen | Quinoline | Automated teller machines | Carbonates | Aldehydes | Hydrogenation | Alcohols
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6. Full Text Selective Catalytic Hydrogenation of Heteroarenes with N‑Graphene-Modified Cobalt Nanoparticles (Co3O4–Co/NGr@α-Al2O3)
by Chen, Feng and Surkus, Annette-Enrica and He, Lin and Pohl, Marga-Martina and Radnik, Jörg and Topf, Christoph and Junge, Kathrin and Beller, Matthias
Journal of the American Chemical Society, ISSN 0002-7863, 09/2015, Volume 137, Issue 36, pp. 11718 - 11724
Cobalt oxide/cobalt-based nanoparticles featuring a core–shell structure and nitrogen-doped graphene layers on alumina are obtained by pyrolysis of... 
HOMOGENEOUS HYDROGENATION | GALIPEA-OFFICINALIS | HIGHLY ENANTIOSELECTIVE HYDROGENATION | RUTHENIUM NANOPARTICLES | IRIDIUM COMPLEXES | QUINOLINE DERIVATIVES | ASYMMETRIC HYDROGENATION | HETEROAROMATIC-COMPOUNDS | CARBONACEOUS MATERIALS | OXIDE CATALYSTS | CHEMISTRY, MULTIDISCIPLINARY
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7. Full Text Mild and Homogeneous Cobalt‐Catalyzed Hydrogenation of CC, CO, and CN Bonds
by Zhang, Guoqi and Scott, Brian L and Hanson, Susan K
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2012, Volume 51, Issue 48, pp. 12102 - 12106
A cationic cobalt(II)–alkyl complex is an effective precatalyst for hydrogenation of alkenes, aldehydes, ketones, and imines under mild conditions (1–4 atm H2;... 
cobalt | homogeneous catalysis | hydrogenation | synthetic methods | MECHANISM | ALKENE HYDROGENATION | CHEMISTRY, MULTIDISCIPLINARY | HYDRIDE COMPLEXES | ALKYL COMPLEXES | 3-COORDINATE | CARBONYL-COMPLEXES | KINETICS | DINITROGEN | CHEMISTRY | ASYMMETRIC HYDROGENATION | Ketones | Alkenes | Imines | Catalysts | Cationic | Tolerances | Catalysis | Hydrogenation
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8. Full Text Ruthenium(II) Complexes Containing Lutidine‐Derived Pincer CNC Ligands: Synthesis, Structure, and Catalytic Hydrogenation of CN bonds
by Hernández‐Juárez, Martín and López‐Serrano, Joaquín and Lara, Patricia and Morales‐Cerón, Judith P and Vaquero, Mónica and Álvarez, Eleuterio and Salazar, Verónica and Suárez, Andrés
Chemistry – A European Journal, ISSN 0947-6539, 05/2015, Volume 21, Issue 20, pp. 7540 - 7555
A series of Ru complexes containing lutidine‐derived pincer CNC ligands have been prepared by transmetalation with the corresponding silver‐carbene... 
carbenes | ligands | ruthenium | homogeneous catalysis | hydrogenation | MOLECULAR-ORBITAL METHODS | ALCOHOL DEHYDROGENATION | N-H | FRUSTRATED LEWIS PAIRS | AROMATIZATION-DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | HETEROCYCLIC-CARBENE COMPLEXES | ACCEPTORLESS DEHYDROGENATION | ASYMMETRIC HYDROGENATION | LATE TRANSITION-METALS | ORGANOMETALLIC CATALYSIS | Imines | Catalysts | Mathematical analysis | Ligands | Derivatives | Catalysis | Hydrogenation | Computer numerical control
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9. Full Text Metal‐Free Catalytic Hydrogenation
by Chase, Preston A and Welch, Gregory C and Jurca, Titel and Stephan, Douglas W
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2007, Volume 46, Issue 42, pp. 8050 - 8053
Phosphonium borates of the form R2PH(C6F4)BH(C6F5)2 are shown to be metal‐free hydrogenation catalysts (see scheme) that effect reduction of sterically... 
dihydrogen | homogeneous catalysis | boron | hydrogenation | phosphorus | Phosphorus | Boron | Dihydrogen | Hydrogenation | Homogeneous catalysis | ACTIVATION | TRIS(PENTAFLUOROPHENYL)BORANE | IMINES | ADDUCTS | AZIRIDINES | BORANES | CHEMISTRY, MULTIDISCIPLINARY | KETONES
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10. Full Text Robust and Porous β‑Diketiminate-Functionalized Metal–Organic Frameworks for Earth-Abundant-Metal-Catalyzed C–H Amination and Hydrogenation
by Thacker, Nathan C and Lin, Zekai and Zhang, Teng and Gilhula, James C and Abney, Carter W and Lin, Wenbin and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Journal of the American Chemical Society, ISSN 0002-7863, 03/2016, Volume 138, Issue 10, pp. 3501 - 3509
We have designed a strategy for postsynthesis installation of the β-diketiminate (NacNac) functionality in a metal–organic framework (MOF) of UiO-topology.... 
OLEFIN HYDROGENATION | BONDS | IRON | IMIDOIRON(III) COMPLEX | LIGAND | CHEMISTRY, MULTIDISCIPLINARY | ASYMMETRIC ALKENE HYDROGENATION | HIGHLY EFFICIENT | TRANSFORMATIONS | ATOM TRANSFER | COBALT | Extended X-ray absorption fine structure | Chemical properties | Research | Chemical compounds | Hydrogenation | Analysis | INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
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11. Full Text Outer sphere hydrogenation catalysis
by Eisenstein, Odile and Crabtree, Robert H
New Journal of Chemistry, ISSN 1144-0546, 2013, Volume 37, Issue 1, pp. 21 - 27
In the title catalysts, the substrate, typically a ketone, imine or N-heterocycle, remains in the outer sphere (OS). The catalyst transfers hydride and a... 
TRANSITION-METAL HYDRIDES | HOMOGENEOUS HYDROGENATION | ASYMMETRIC TRANSFER HYDROGENATION | N-HETEROCYCLIC CARBENE | PRIMARY AMINE DONOR | HYDROXYCYCLOPENTADIENYL RUTHENIUM HYDRIDE | DIHYDROGEN ACTIVATION | IONIC HYDROGENATION | FRUSTRATED LEWIS PAIRS | CARBON-DIOXIDE | CHEMISTRY, MULTIDISCIPLINARY | Chemical Sciences | Coordination chemistry
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