Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 35 checked references that resolve
resolves10.1002/adsc.200390030Ruthenium(II)‐Catalyzed Asymmetric Transfer Hydrogenation of Carbonyl Compounds with 2‐Propanol and Ephedrine‐Type Ligands
resolves10.1016/j.ccr.2004.04.007Mechanisms of the H2-hydrogenation and transfer hydrogenation of polar bonds catalyzed by ruthenium hydride complexes
resolves10.1039/B513396CAsymmetric transfer hydrogenation: chiral ligands and applications
resolves10.1021/ar700134qAsymmetric Transfer Hydrogenation of Ketones with Bifunctional Transition Metal-Based Molecular Catalysts
resolves10.1021/ar9502341Asymmetric Transfer Hydrogenation Catalyzed by Chiral Ruthenium Complexes
resolves10.1039/b515269kMechanistic aspects of transition metal-catalyzed hydrogen transfer reactions
resolves10.1039/c3cy00854aSelective catalytic transfer hydrogenation of nitriles to primary amines using Pd/C
resolves10.1016/j.molcata.2012.10.010Reduction of citral in water under typical transfer hydrogenation conditions—Reaction mechanisms with evolution of and hydrogenation by molecular hydrogen
resolves10.1016/j.jhazmat.2011.11.089Reduction of benzo[a]pyrene with acid-activated magnesium metal in ethanol: A possible application for environmental remediation
resolves10.1021/cs200299vPotassium Phosphate as a Solid Base Catalyst for the Catalytic Transfer Hydrogenation of Aldehydes and Ketones
resolves10.1016/j.apcata.2010.01.004Water-improved heterogeneous transfer hydrogenation using methanol as hydrogen donor over Pd-based catalyst
resolves10.1016/j.poly.2010.11.037NiO nanoparticles prepared via thermal decomposition of the bis(dimethylglyoximato)nickel(II) complex: A novel reusable heterogeneous catalyst for fast and efficient microwave-assisted reduction of nitroarenes with ethanol
resolves10.1016/j.apcata.2014.07.010Highly efficient transfer hydrogenation of aldehydes and ketones using potassium formate over AlO(OH)-entrapped ruthenium catalysts
resolves10.1016/j.jtice.2016.05.032Using decalin and tetralin as hydrogen source for transfer hydrogenation of renewable lignin-derived phenolics over activated carbon supported Pd and Pt catalysts
resolves10.1039/C5RA00367ACatalytic hydrogenation of phenol, cresol and guaiacol over physically mixed catalysts of Pd/C and zeolite solid acids
resolves10.1007/s11814-017-0126-xUpgrading of pyrolysis bio-oil using WO3/ZrO2 and Amberlyst catalysts: Evaluation of acid number and viscosity
resolves10.1039/C5RA22137DEffective parameters on selective catalytic hydrodeoxygenation of phenolic compounds of pyrolysis bio-oil to high-value hydrocarbons
resolves10.1016/j.fuproc.2015.04.023Catalytic transfer hydrogenation for stabilization of bio-oil oxygenates: Reduction of p-cresol and furfural over bimetallic Ni–Cu catalysts using isopropanol
resolves10.1016/j.renene.2016.12.054In situ catalytic hydrogenation of model compounds and biomass-derived phenolic compounds for bio-oil upgrading
resolves10.1002/ep.11915Upgrading bio‐oil model compounds phenol and furfural with <i>in situ</i> generated hydrogen
resolves10.1016/j.apcata.2015.04.009Selective transfer hydrogenation of phenol to cyclohexanone on supported palladium catalyst using potassium formate as hydrogen source under open atmosphere
resolves10.1039/C6RA24218AExploratory catalyst screening studies on the liquefaction of model humins from C6 sugars
resolves10.1139/v78-415The formation of propane, propylene, and acetone from 2-propanol over vanadium pentoxide and modified vanadium pentoxide catalysts
resolves10.1039/C5RA12844G<i>In situ</i>
hydrogenation of furfural with additives over a RANEY® Ni catalyst
resolves10.1016/j.biortech.2011.06.015One-step hydrogenation–esterification of furfural and acetic acid over bifunctional Pd catalysts for bio-oil upgrading
resolves10.1039/c2ee21855kExploiting H-transfer reactions with RANEY® Ni for upgrade of phenolic and aromatic biorefinery feeds under unusual, low-severity conditions
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