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 41 checked references that resolve
resolves10.1021/cr050989dChemical Routes for the Transformation of Biomass into Chemicals
resolves10.1002/ceat.200700417The Roll of Chemocatalysis in the Establishment of the Technology Platform “Renewable Resources”
resolves10.1039/b922014cTechnology development for the production of biobased products from biorefinery carbohydrates—the US Department of Energy’s “Top 10” revisited
resolves10.1021/la101424aγ-Valerolactone Ring-Opening and Decarboxylation over SiO<sub>2</sub>/Al<sub>2</sub>O<sub>3</sub> in the Presence of Water
resolves10.1039/B712863Kγ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals
resolves10.1021/ja01370a069NORMAL VALEROLACTONE. III. ITS PREPARATION BY THE CATALYTIC REDUCTION OF LEVULINIC ACID WITH HYDROGEN IN THE PRESENCE OF PLATINUM OXIDE
resolves10.1021/ja01200a036Derivatives of γ-Valerolactone, 1,4-Pentanediol and 1,4-Di-(β-cyanoethoxy)-pentane<sup>1</sup>
resolves10.1021/ef900259hSynthesis of γ-Valerolactone by Hydrogenation of Biomass-derived Levulinic Acid over Ru/C Catalyst
resolves10.1039/c2gc15872hA sustainable process for the production of γ-valerolactone by hydrogenation of biomass-derived levulinic acid
resolves10.1007/s11244-008-9047-6Integration of Homogeneous and Heterogeneous Catalytic Processes for a Multi-step Conversion of Biomass: From Sucrose to Levulinic Acid, γ-Valerolactone, 1,4-Pentanediol, 2-Methyl-tetrahydrofuran, and Alkanes
resolves10.1039/b904693cCombined dehydration/(transfer)-hydrogenation of C6-sugars (D-glucose and D-fructose) to γ-valerolactone using ruthenium catalysts
resolves10.1039/b708754cMaximising opportunities in supercritical chemistry: the continuous conversion of levulinic acid to γ-valerolactone in CO2
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/S0022-328X(00)89230-XPreparation and properties of hydride triphenyl-phosphine ruthenium complexes with 3-formyl (or acyl) propionate [RuH(ocochrchrcor′)(PPh3)3] (R H, CH3, C2H5; R H, CH3, C6H5) and with 2-formyl (or acyl) benzoate [RuH(o-OCCOC6H4COR′)(PPh3)3] (R′ H, CH3)
resolves10.1002/anie.200902281Catalytic Conversion of Biomass‐Derived Carbohydrates into γ‐Valerolactone without Using an External H<sub>2</sub> Supply
resolves10.1038/nmat1916Enhanced ethanol production inside carbon-nanotube reactors containing catalytic particles
resolves10.1021/ja8008192Effect of Confinement in Carbon Nanotubes on the Activity of Fischer−Tropsch Iron Catalyst
resolves10.1002/anie.200352275Chemoselective Reduction of Complex α,β‐Unsaturated Ketones to Allylic Alcohols over Ir‐Metal Particles on β Zeolites
resolves10.1016/S0926-860X(99)00229-XPreparation, characterization and catalytic hydroformylation properties of carbon nanotubes-supported Rh–phosphine catalyst
resolves10.1021/ar000145aDevelopment of Novel Lewis Acid Catalysts for Selective Organic Reactions in Aqueous Media
resolves10.1021/jp800152fSynthesis and Characterization of Dendrimer-Derived Supported Iridium Catalysts
resolves10.1007/s10562-007-9051-7Supported iridium catalysts prepared by atomic layer deposition: effect of reduction and calcination on activity in toluene hydrogenation
resolves10.1021/ja00096a076Application of Carbon Nanotubes as Supports in Heterogeneous Catalysis
resolves10.1021/ja055530fMicroemulsion-Templated Synthesis of Carbon Nanotube-Supported Pd and Rh Nanoparticles for Catalytic Applications
resolves10.1039/b507765fCarbon nanotube-promoted Co–Cu catalyst for highly efficient synthesis of higher alcohols from syngas
resolves10.1002/anie.200805715Ruthenium Nanoparticles Supported on Carbon Nanotubes as Efficient Catalysts for Selective Conversion of Synthesis Gas to Diesel Fuel
resolves10.1002/anie.200705972Controlled Generation of Hydrogen from Formic Acid Amine Adducts at Room Temperature and Application in H<sub>2</sub>/O<sub>2</sub> Fuel Cells
The 7 references without a DOI — listed, not checked
no DOI — not checked10.1016/S1872-2067(11)60522-6_bib1
no DOI — not checked10.1016/S1872-2067(11)60522-6_bib3
no DOI — not checkedDunlop A P, Madden J W. US Patent 2786852. 1957
no DOI — not checkedFitzpatrick S W. US Patent 5608105. 1997
no DOI — not checked10.1016/S1872-2067(11)60522-6_bib32
no DOI — not checked10.1016/S1872-2067(11)60522-6_bib44
no DOI — not checked10.1016/S1872-2067(11)60522-6_bib48
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