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 73 checked references that resolve
resolves10.1016/j.catcom.2014.11.009Pd/C catalyzed conversion of levulinic acid to γ-valerolactone using alcohol as a hydrogen donor under microwave conditions
resolves10.1007/s12039-018-1418-3Formic acid assisted hydrogenation of levulinic acid to $$\upgamma $$ γ -valerolactone over ordered mesoporous $$\hbox {Cu/Fe}_{2}\hbox {O}_{3}$$ Cu/Fe 2 O 3 catalyst prepared by hard template method
resolves10.1002/cssc.201403398Selective Hydrogenation of Furfural to Furfuryl Alcohol in the Presence of a Recyclable Cobalt/SBA‐15 Catalyst
resolves10.1039/C8RA01316KSupported cobalt catalysts for the selective hydrogenation of ethyl levulinate to various chemicals
resolves10.1021/op068002cRecent Developments In Meerwein−Ponndorf−Verley and Related Reactions for the Reduction of Organic Functional Groups Using Aluminum, Boron, and Other Metal Reagents: A Review
resolves10.1039/c1cc14748jLiquid-phase catalytic transfer hydrogenation and cyclization of levulinic acid and its esters to γ-valerolactone over metal oxide catalysts
resolves10.1002/cssc.201000163Conversion of Levulinic Acid and Formic Acid into γ‐Valerolactone over Heterogeneous Catalysts
resolves10.1002/anie.201100102Hydrogen‐Independent Reductive Transformation of Carbohydrate Biomass into γ‐Valerolactone and Pyrrolidone Derivatives with Supported Gold Catalysts
resolves10.1016/j.jcat.2018.09.025Catalytic transfer hydrogenation of biomass-derived furfural to furfuryl alcohol over in-situ prepared nano Cu-Pd/C catalyst using formic acid as hydrogen source
resolves10.1016/j.cej.2019.04.199Green synthesis of gamma-valerolactone (GVL) through hydrogenation of biomass-derived levulinic acid using non-noble metal catalysts: A critical review
resolves10.1021/acscatal.5b02171Heterogeneous Catalytic Transfer Hydrogenation as an Effective Pathway in Biomass Upgrading
resolves10.1002/cssc.201501402Recyclable Earth‐Abundant Metal Nanoparticle Catalysts for Selective Transfer Hydrogenation of Levulinic Acid to Produce <i>γ</i>‐Valerolactone
resolves10.1016/j.cej.2017.07.145Levulinic acid hydrodeoxygenation, decarboxylation and oligmerization over NiMo/Al2O3 catalyst to bio-based value-added chemicals: Modelling of mass transfer, thermodynamics and micro-kinetics
resolves10.1007/s10562-018-2618-7Screening of Solvents, Hydrogen Source, and Investigation of Reaction Mechanism for the Hydrocyclisation of Levulinic Acid to γ-Valerolactone Using Ni/SiO2–Al2O3 Catalyst
resolves10.1016/j.supflu.2018.11.010Hydrogen gas-free processes for single-step preparation of transition-metal bifunctional catalysts and one-pot γ-valerolactone synthesis in supercritical CO2-ionic liquid systems
resolves10.1039/c3ra46495dSurface synergism of an Ag–Ni/ZrO2 nanocomposite for the catalytic transfer hydrogenation of bio-derived platform molecules
resolves10.1016/j.cej.2018.07.007Catalytic transfer hydrogenation of biomass-derived 5-hydroxymethylfurfural into 2,5-dihydroxymethylfuran over magnetic zirconium-based coordination polymer
resolves10.1002/slct.201800536Synthesis of γ‐Valerolactone from Levulinic Acid and Formic Acid over Mg‐Al Hydrotalcite Like Compound
resolves10.1016/j.apcatb.2018.11.035Metal-organic framework derived Ni/NiO micro-particles with subtle lattice distortions for high-performance electrocatalyst and supercapacitor
resolves10.1021/cs400572qRhenium-Catalyzed Acceptorless Dehydrogenative Coupling via Dual Activation of Alcohols and Carbonyl Compounds
resolves10.1002/cssc.201801620Catalytic Transfer Hydrogenation of Biomass‐Derived Substrates to Value‐Added Chemicals on Dual‐Function Catalysts: Opportunities and Challenges
resolves10.1007/s12540-013-6033-8Effect of the valence states of titanium on the lattice structure and ionic conductivity of Li0.33La0.55TiO3 solid electrolyte
resolves10.1016/j.jiec.2017.12.020Selective hydrogenation of biomass-derived ethyl levulinate to γ-valerolactone over supported Co catalysts in continuous process at atmospheric pressure
resolves10.1039/b924648gTransfer hydrogenation of levulinic acid under hydrothermal conditions catalyzed by sulfate as a temperature-switchable base
resolves10.1021/acssuschemeng.6b02464Catalytic Transfer Hydrogenation of Biomass-Derived Levulinic Acid and Its Esters to γ-Valerolactone over Sulfonic Acid-Functionalized UiO-66
resolves10.1039/C6GC01296EMagnetic ZSM-5 zeolite: a selective catalyst for the valorization of furfuryl alcohol to γ-valerolactone, alkyl levulinates or levulinic acid
resolves10.1021/jacs.6b00858Heterogeneous Spin States in Ultrathin Nanosheets Induce Subtle Lattice Distortion To Trigger Efficient Hydrogen Evolution
resolves10.1039/C7CY00902JEffect of SiO
<sub>2</sub>
support properties on the performance of Cu–SiO
<sub>2</sub>
catalysts for the hydrogenation of levulinic acid to gamma valerolactone using formic acid as a hydrogen source
resolves10.1007/s10562-017-2241-zVapor Phase Catalytic Transfer Hydrogenation (CTH) of Levulinic Acid to γ-Valerolactone Over Copper Supported Catalysts Using Formic Acid as Hydrogen Source
resolves10.1002/cssc.201402699Cobalt–Manganese‐Based Spinels as Multifunctional Materials that Unify Catalytic Water Oxidation and Oxygen Reduction Reactions
resolves10.1039/C5CC02993GConversion of levulinic acid into γ-valerolactone using Fe
<sub>3</sub>
(CO)
<sub>12</sub>
: mimicking a biorefinery setting by exploiting crude liquors from biomass acid hydrolysis
resolves10.1039/C7GC00027HMnCo
<sub>2</sub>
O
<sub>4</sub>
spinel supported ruthenium catalyst for air-oxidation of HMF to FDCA under aqueous phase and base-free conditions
resolves10.1016/j.jiec.2017.11.040Facile production of 2,5-diformylfuran from base-free oxidation of 5-hydroxymethyl furfural over manganese–cobalt spinels supported ruthenium nanoparticles
resolves10.1080/08927022.2019.1632448Predicting CO<sub>2</sub> adsorption and reactivity on transition metal surfaces using popular density functional theory methods
resolves10.1002/slct.201803645Magnesium Aluminate Supported Cu Catalyst for Selective Transfer Hydrogenation of Biomass Derived Furfural to Furfuryl Alcohol with Formic Acid as Hydrogen Donor
resolves10.1002/cssc.201600751The Role of the Hydrogen Source on the Selective Production of γ‐Valerolactone and 2‐Methyltetrahydrofuran from Levulinic Acid
resolves10.1002/jctb.5213Recent advances in the production of γ‐valerolactone from biomass‐derived feedstocks via heterogeneous catalytic transfer hydrogenation
resolves10.1016/j.ijhydene.2012.11.006Role of particle size, grain size, microstrain and lattice distortion in improved dehydrogenation properties of the ball-milled Mg(AlH4)2
resolves10.1039/C5GC02200BRu catalysts for levulinic acid hydrogenation with formic acid as a hydrogen source
resolves10.1021/ie100598aHydrogen-Transfer Reduction of Ketones into Corresponding Alcohols Using Formic Acid as a Hydrogen Donor without a Metal Catalyst in High-Temperature Water
resolves10.1002/anie.201504001Porous Zirconium–Phytic Acid Hybrid: a Highly Efficient Catalyst for Meerwein–Ponndorf–Verley Reductions
resolves10.1021/acssuschemeng.8b03211Chlorine Influence on Palladium Doped Nickel Catalysts in Levulinic Acid Hydrogenation with Formic Acid as Hydrogen Source
resolves10.1021/cs501409sStabilization of Cobalt Catalysts by Embedment for Efficient Production of Valeric Biofuel
resolves10.1016/j.rser.2014.07.209Production of γ-valerolactone from lignocellulosic biomass for sustainable fuels and chemicals supply
resolves10.1002/cctc.201500115In Situ Generated Catalyst System to Convert Biomass‐Derived Levulinic Acid to γ‐Valerolactone
resolves10.1016/j.apcata.2014.12.007Nickel-promoted copper–silica nanocomposite catalysts for hydrogenation of levulinic acid to lactones using formic acid as a hydrogen feeder
resolves10.1039/C9EE01747JFormic acid, a biomass-derived source of energy and hydrogen for biomass upgrading
resolves10.1039/C5NJ02655EGas phase hydrogenation of levulinic acid to γ-valerolactone over supported Ni catalysts with formic acid as hydrogen source
resolves10.1002/ceat.201600429Hydrogenation of Levulinic Acid Using Formic Acid as a Hydrogen Source over Ni/SiO<sub>2</sub> Catalysts
resolves10.1016/S1872-2067(18)63105-5An efficient and reusable bimetallic Ni3Fe NPs@C catalyst for selective hydrogenation of biomass-derived levulinic acid to γ-valerolactone
resolves10.1039/C4RA01120AZirconium–Beta zeolite as a robust catalyst for the transformation of levulinic acid to γ-valerolactone via Meerwein–Ponndorf–Verley reduction
resolves10.1039/C7CC05007KRobust synthesis of green fuels from biomass-derived ethyl esters over a hierarchically core/shell-structured ZSM-5@(Co/SiO
<sub>2</sub>
) catalyst
resolves10.1002/cssc.201801974Enhanced Production of γ‐Valerolactone with an Internal Source of Hydrogen on Ca‐Modified TiO<sub>2</sub> Supported Ru Catalysts
resolves10.1021/acscatal.7b02837Synergetic Catalysis of Bimetallic CuCo Nanocomposites for Selective Hydrogenation of Bioderived Esters
resolves10.1002/cssc.201800667Highly Active Catalytic Ruthenium/TiO<sub>2</sub> Nanomaterials for Continuous Production of γ‐Valerolactone
resolves10.1039/C7GC02503CConversion of levulinic acid and alkyl levulinates into biofuels and high-value chemicals
resolves10.1039/c3cc40980eRANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature
resolves10.3390/app5030532Microwave-Assisted Conversion of Levulinic Acid to γ-Valerolactone Using Low-Loaded Supported Iron Oxide Nanoparticles on Porous Silicates
resolves10.1039/c3ee40857dCopper-based catalysts for the efficient conversion of carbohydrate biomass into γ-valerolactone in the absence of externally added hydrogen
resolves10.1039/C5GC02971FHydrogenative cyclization of levulinic acid into γ-valerolactone by photocatalytic intermolecular hydrogen transfer
resolves10.1016/j.cattod.2018.08.011Novel and efficient cobalt catalysts synthesized by one-step solution phase reduction for the conversion of biomass derived ethyl levulinate
resolves10.1039/C4GC00482ECobalt catalysts: very efficient for hydrogenation of biomass-derived ethyl levulinate to gamma-valerolactone under mild conditions
resolves10.1039/C4RA14363AOne-pot conversion of carbohydrates into gamma-valerolactone catalyzed by highly cross-linked ionic liquid polymer and Co/TiO
<sub>2</sub>
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