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 125 checked references that resolve
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resolves10.1021/sc500664hCellulose–Hemicellulose and Cellulose–Lignin Interactions during Fast Pyrolysis
resolves10.1039/C8GC00234GCatalytic conversion of 5-hydroxymethylfurfural to some value-added derivatives
resolves10.1021/acs.chemrev.8b00134How Catalysts and Experimental Conditions Determine the Selective Hydroconversion of Furfural and 5-Hydroxymethylfurfural
resolves10.1002/cctc.201701754Metal Catalysts for the Efficient Transformation of Biomass‐derived HMF and Furfural to Value Added Chemicals
resolves10.1039/C7GC02503CConversion of levulinic acid and alkyl levulinates into biofuels and high-value chemicals
resolves10.1039/C8GC02001AValorization of levulinic acid over non-noble metal catalysts: challenges and opportunities
resolves10.1021/acscatal.7b03530Catalytic Advances in the Production and Application of Biomass-Derived 2,5-Dihydroxymethylfuran
resolves10.1039/C5EE02666KFurfural: a renewable and versatile platform molecule for the synthesis of chemicals and fuels
resolves10.1039/D0CS00041HRecent catalytic routes for the preparation and the upgrading of biomass derived furfural and 5-hydroxymethylfurfural
resolves10.1021/acscatal.5b02171Heterogeneous Catalytic Transfer Hydrogenation as an Effective Pathway in Biomass Upgrading
resolves10.1002/cssc.202000175Heterogeneous Catalytic Hydrogenation of Levulinic Acid to γ‐Valerolactone with Formic Acid as Internal Hydrogen Source
resolves10.1039/b922014cTechnology development for the production of biobased products from biorefinery carbohydrates—the US Department of Energy’s “Top 10” revisited
resolves10.1007/s10098-018-1568-5An overview of biorefinery-derived platform chemicals from a cellulose and hemicellulose biorefinery
resolves10.1021/acscatal.6b01838Furfural: A Promising Platform Compound for Sustainable Production of C<sub>4</sub> and C<sub>5</sub> Chemicals
resolves10.1038/srep28558Highly selective hydrogenation of furfural to furfuryl alcohol over Pt nanoparticles supported on g-C3N4 nanosheets catalysts in water
resolves10.1016/j.clay.2019.105351Catalytic transfer hydrogenation of furfural to furfuryl alcohol over calcined MgFe hydrotalcites
resolves10.1021/acssuschemeng.6b02272Catalytic Transfer Hydrogenation of Furfural into Furfuryl Alcohol over Magnetic γ-Fe<sub>2</sub>O<sub>3</sub>@HAP Catalyst
resolves10.1021/cs300395aDFT Study of Furfural Conversion to Furan, Furfuryl Alcohol, and 2-Methylfuran on Pd(111)
resolves10.1021/cs200336rUnderstanding and Controlling Reactivity of Unsaturated Oxygenates and Polyols on Metal Catalysts
resolves10.1021/nl3023127High Structure Sensitivity of Vapor-Phase Furfural Decarbonylation/Hydrogenation Reaction Network as a Function of Size and Shape of Pt Nanoparticles
resolves10.1007/s10562-008-9754-4Dependence of Gas-Phase Crotonaldehyde Hydrogenation Selectivity and Activity on the Size of Pt Nanoparticles (1.7–7.1 nm) Supported on SBA-15
resolves10.1021/ja0012974Supported Gold Nanoparticles from Quantum Dot to Mesoscopic Size Scale: Effect of Electronic and Structural Properties on Catalytic Hydrogenation of Conjugated Functional Groups
resolves10.1016/j.jcat.2005.09.023Selective hydrogenation of α,βα,β-unsaturated ketone to α,βα,β-unsaturated alcohol on gold-supported iron oxide catalysts: Role of the support
resolves10.1021/ja306079hFurfuraldehyde Hydrogenation on Titanium Oxide-Supported Platinum Nanoparticles Studied by Sum Frequency Generation Vibrational Spectroscopy: Acid–Base Catalysis Explains the Molecular Origin of Strong Metal–Support Interactions
resolves10.1021/cs500620bTotal Hydrogenation of Furfural and 5-Hydroxymethylfurfural over Supported Pd–Ir Alloy Catalyst
resolves10.1002/cctc.201500097Robust and Recyclable Nonprecious Bimetallic Nanoparticles on Carbon Nanotubes for the Hydrogenation and Hydrogenolysis of 5‐Hydroxymethylfurfural
resolves10.1021/acscatal.5b00038Deoxygenation of Biomass-Derived Oxygenates: Reaction of Furfural on Zn-Modified Pt(111)
resolves10.1021/cs500598yEffects of Thiol Modifiers on the Kinetics of Furfural Hydrogenation over Pd Catalysts
resolves10.1021/acssuschemeng.6b02343Efficient Synthesis of Furfuryl Alcohol from H<sub>2</sub>-Hydrogenation/Transfer Hydrogenation of Furfural Using Sulfonate Group Modified Cu Catalyst
resolves10.1016/j.mcat.2017.11.011Efficient catalytic transfer hydrogenation of furfural to furfuryl alcohol in near-critical isopropanol over Cu/MgO-Al2O3 catalyst
resolves10.3390/catal8110539MPV Reduction of Furfural to Furfuryl Alcohol on Mg, Zr, Ti, Zr–Ti, and Mg–Ti Solids: Influence of Acid–Base Properties
resolves10.3390/ijms20040828Influence of Structure-modifying Agents in the Synthesis of Zr-doped SBA-15 Silica and Their Use as Catalysts in the Furfural Hydrogenation to Obtain High Value-added Products through the Meerwein-Ponndorf-Verley Reduction
resolves10.1002/cctc.201902033Catalytic Transfer Hydrogenation of Furfural over Co<sub>3</sub>O<sub>4</sub>−Al<sub>2</sub>O<sub>3</sub> Hydrotalcite‐derived Catalyst
resolves10.1002/cctc.201701266Catalytic Transfer Hydrogenation of Furfural to Furfuryl Alcohol with Recyclable Al–Zr@Fe Mixed Oxides
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
resolves10.1016/j.fuproc.2019.106205Selective hydrogenation of furfural to furfuryl alcohol without external hydrogen over N-doped carbon confined Co catalysts
resolves10.1021/acscatal.5b00586Mechanistic Insights into Metal Lewis Acid-Mediated Catalytic Transfer Hydrogenation of Furfural to 2-Methylfuran
resolves10.1039/C9EE01747JFormic acid, a biomass-derived source of energy and hydrogen for biomass upgrading
resolves10.1002/cssc.201300774Catalytic Transfer Hydrogenation/Hydrogenolysis for Reductive Upgrading of Furfural and 5‐(Hydroxymethyl)furfural
resolves10.1016/j.fuel.2012.05.043Combustion characteristics and emissions of 2-methylfuran compared to 2,5-dimethylfuran, gasoline and ethanol in a DISI engine
resolves10.1016/j.rser.2014.07.003Production, properties and catalytic hydrogenation of furfural to fuel additives and value-added chemicals
resolves10.3390/catal8080313Catalytic Transfer Hydrogenolysis as an Effective Tool for the Reductive Upgrading of Cellulose, Hemicellulose, Lignin, and Their Derived Molecules
resolves10.1021/acssuschemeng.7b00778Selective Transfer Hydrogenation of Biomass-Based Furfural and 5-Hydroxymethylfurfural over Hydrotalcite-Derived Copper Catalysts Using Methanol as a Hydrogen Donor
resolves10.1016/j.apcata.2018.11.029Catalytic in-situ hydrogenation of 5-hydroxymethylfurfural to 2,5-dimethylfuran over Cu-based catalysts with methanol as a hydrogen donor
resolves10.1021/acssuschemeng.8b02425Selective Deoxygenation of Aqueous Furfural to 2-Methylfuran over Cu<sup>0</sup>/Cu<sub>2</sub>O·SiO<sub>2</sub> Sites via a Copper Phyllosilicate Precursor without Extraneous Gas
resolves10.1016/j.apcatb.2018.01.006Nitrogen-doped carbon-decorated copper catalyst for highly efficient transfer hydrogenolysis of 5-hydroxymethylfurfural to convertibly produce 2,5-dimethylfuran or 2,5-dimethyltetrahydrofuran
resolves10.1016/j.apcata.2017.09.011High efficient conversion of furfural to 2-methylfuran over Ni-Cu/Al2O3 catalyst with formic acid as a hydrogen donor
resolves10.1016/j.fuel.2016.09.026Catalytic transfer hydrogenation/hydrogenolysis of 5-hydroxymethylfurfural to 2,5-dimethylfuran over Ni-Co/C catalyst
resolves10.1039/c3gc37065hGamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
resolves10.1002/cssc.201200111Development of Heterogeneous Catalysts for the Conversion of Levulinic Acid to γ‐Valerolactone
resolves10.1039/C6RA08637CTransfer hydrogenation of biomass-derived levulinic acid to γ-valerolactone over supported Ni catalysts
resolves10.1016/j.catcom.2019.03.021Facile synthesis of γ-valerolactone by transfer hydrogenation of methyl levulinate and levulinic acid over Ni/ZrO2
resolves10.1039/C6RA25594ACatalytic transfer hydrogenation of levulinic acid to γ-valerolactone over a bifunctional tin catalyst
resolves10.1021/acs.iecr.0c00257Catalytic Transfer Hydrogenation of Levulinic Acid to γ-Valerolactone over Ni<sub>3</sub>P-CePO<sub>4</sub> Catalysts
resolves10.1016/j.indcrop.2020.112133Efficient transfer hydrogenation of biomass derived furfural and levulinic acid via magnetic zirconium nanoparticles: Experimental and kinetic study
resolves10.1039/C5RA27513JZrO
<sub>2</sub>
/SBA-15 as an efficient catalyst for the production of γ-valerolactone from biomass-derived levulinic acid in the vapour phase at atmospheric pressure
resolves10.1039/c3ee40857dCopper-based catalysts for the efficient conversion of carbohydrate biomass into γ-valerolactone in the absence of externally added hydrogen
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
resolves10.1016/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/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
resolves10.1021/acssuschemeng.9b00778Transfer Hydrogenation of Methyl and Ethyl Levulinate Promoted by a ZrO<sub>2</sub> Catalyst: Comparison of Batch vs Continuous Gas-Flow Conditions
resolves10.1021/acssuschemeng.8b00549Continuous Flow Conversion of Biomass-Derived Methyl Levulinate into γ-Valerolactone Using Functional Metal Organic Frameworks
resolves10.1039/C6GC00524ACatalytic transfer hydrogenation of ethyl levulinate to γ-valerolactone over zirconium-based metal–organic frameworks
resolves10.1039/C8SE00098KIntegration of a metal–organic framework with zeolite: a highly sustainable composite catalyst for the synthesis of γ-valerolactone and coumarins
resolves10.1016/j.apcatb.2013.10.021Conversion of biomass to γ-valerolactone by catalytic transfer hydrogenation of ethyl levulinate over metal hydroxides
resolves10.1016/j.mcat.2017.09.011Catalytic transfer hydrogenation of ethyl levulinate to γ-valerolactone over a novel porous Zirconium trimetaphosphate
resolves10.1002/slct.201904480One‐Pot Transfer Hydrogenation of methyl levulinate into valerolactone and 1,4‐pentanediol over in situ Reduced Cu/ZrOCO3 in 2‐PrOH
resolves10.1021/acsomega.6b00469Porous Ti/Zr Microspheres for Efficient Transfer Hydrogenation of Biobased Ethyl Levulinate to γ-Valerolactone
resolves10.1021/acs.iecr.9b01774Hierarchical Flower-like Bimetallic NiCu catalysts for Catalytic Transfer Hydrogenation of Ethyl Levulinate into γ-Valerolactone
resolves10.1021/acssuschemeng.6b01677Enhanced Catalytic Transfer Hydrogenation of Ethyl Levulinate to γ-Valerolactone over a Robust Cu–Ni Bimetallic Catalyst
resolves10.1002/jctb.5213Recent advances in the production of γ‐valerolactone from biomass‐derived feedstocks via heterogeneous catalytic transfer hydrogenation
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
resolves10.1038/nnano.2011.42Hydrogen production from formic acid decomposition at room temperature using a Ag–Pd core–shell nanocatalyst
resolves10.1039/c2gc35881fProduction of butene oligomers as transportation fuels using butene for esterification of levulinic acid from lignocellulosic biomass: process synthesis and technoeconomic evaluation
resolves10.1126/science.1184362Integrated Catalytic Conversion of γ-Valerolactone to Liquid Alkenes for Transportation Fuels
resolves10.1039/C9SE01287GFast and efficient upgrading of levulinic acid into long-chain alkyl levulinate fuel additives with a tungsten salt catalyst at low temperature
resolves10.1039/C6SE00103CConversion of furfuryl alcohol to alkyl levulinate fuel additives over Al
<sub>2</sub>
O
<sub>3</sub>
/SBA-15 catalyst
resolves10.1021/cr5001892Understanding TiO<sub>2</sub>Photocatalysis: Mechanisms and Materials
resolves10.1039/C7GC03522EPhotocatalytic conversion of biomass into valuable products: a meaningful approach?
resolves10.1246/cl.171053Photocatalytic Selective Hydrogenation of Furfural to Furfuryl Alcohol over Titanium(IV) Oxide
resolves10.1021/acssuschemeng.9b01305Cu/Cu<sub>2</sub>O-MC (MC = Mesoporous Carbon) for Highly Efficient Hydrogenation of Furfural to Furfuryl Alcohol under Visible Light
resolves10.1039/C9GC03019KSelective hydrogenation
<i>via</i>
cascade catalysis on amorphous TiO
<sub>2</sub>
resolves10.1021/acs.oprd.8b00428Efficient Electrocatalytic Reduction of Furfural to Furfuryl Alcohol in a Microchannel Flow Reactor
resolves10.1021/jacs.7b06331Mechanisms of Furfural Reduction on Metal Electrodes: Distinguishing Pathways for Selective Hydrogenation of Bioderived Oxygenates
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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