About: γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals

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article by István T. Horváth et al published 2008 in Green Chemistry

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2008 (fr) наукова стаття, опублікована у 2008 (uk) im Jahr 2008 veröffentlichter wissenschaftlicher Artikel (de) article by István T. Horváth et al published 2008 in Green Chemistry (en)
publication date	wds:Q56681326-8129D7EF-B4C7-4E0C-9385-97D193C63E48
publication date	2008-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56681326-78E5E6A8-37A2-4FB0-8B68-1C03203EE75E
language of work or name	English
author name string	wds:Q56681326-5CC432F3-F4E5-4731-A27A-A851CAE8AC4E wds:Q56681326-778AE8F7-04D0-4B9E-AF58-E946A793705B wds:Q56681326-DCD2C680-2F09-4961-A357-59F125CDBB11 wds:Q56681326-DDBEA0E0-A6B5-49C8-988E-813B329607EB wds:Q56681326-EF4AF33E-B24F-490F-AD22-B86974A79564
author name string	István T. Horváth Hasan Mehdi Viktória Fábos László T. Mika László Boda
rdfs:label	γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (en) γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (nl)
skos:prefLabel	γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (en) γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (nl)
name	γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (en) γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (nl)
title	wds:Q56681326-9942460C-A2AD-4549-AABD-B8D29282CF6C
title	γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals (en)
page(s)	wds:Q56681326-7F5FC9B6-93F2-46E8-A5B9-EC5E4B6BD229
page(s)	238-242
instance of	wds:Q56681326-22C891A4-64F2-4F73-9B66-F151DECCD0B4
instance of	scholarly article
main subject	wds:Q56681326-04B0A131-032A-4EFB-A75E-54294F0A28B0
main subject	liquid
published in	wds:Q56681326-AE9B9AB7-0048-4CAE-83E7-58769A0AC972
published in	Green Chemistry
issue	wds:Q56681326-3C8450E3-33A1-4EDC-8B46-9C037017AB9D
volume	wds:Q56681326-3CF71E35-7429-4A71-B9C3-D35E3090CD0F
issue	2
volume	10
DOI	wds:Q56681326-4ECAEA23-0EDD-404A-8C73-6D3B0831D5C8
DOI	http://dx.doi.org/10.1039/B712863K
DOI	10.1039/B712863K
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56681326
is cites work of	Hydrodeoxygenation of the angelica lactone dimer, a cellulose-based feedstock: simple, high-yield synthesis of branched C7 -C10 gasoline-like hydrocarbons. Valorization of biomass: deriving more value from waste Transformations of biomass-derived platform molecules: from high added-value chemicals to fuels via aqueous-phase processing. Conversion of levulinic acid and formic acid into γ-valerolactone over heterogeneous catalysts Efficient route to hydroxymethylfurans from sugars via transfer hydrogenation Opportunities for Bio-Based Solvents Created as Petrochemical and Fuel Products Transition towards Renewable Resources Bio-based solvents: an emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry. Heterogeneous catalysis and the challenges of powering the planet, securing chemicals for civilised life, and clean efficient utilization of renewable feedstocks Potential and challenges of zeolite chemistry in the catalytic conversion of biomass. Domino reaction catalyzed by zeolites with Brønsted and Lewis acid sites for the production of γ-valerolactone from furfural. Development of heterogeneous catalysts for the conversion of levulinic acid to γ-valerolactone Biorefineries for the production of top building block chemicals and their derivatives Direct conversion of cellulose to levulinic acid and gamma-valerolactone using solid acid catalysts Synthesis of γ-Valerolactone from Carbohydrates and its Applications Conversion of carbohydrate biomass to γ-valerolactone by using water-soluble and reusable iridium complexes in acidic aqueous media Ionic-liquid-catalyzed efficient transformation of γ-valerolactone to methyl 3-pentenoate under mild conditions Cascade upgrading of γ-valerolactone to biofuels Advanced biorefinery based on the fractionation of biomass in γ-valerolactone and water Production of levulinic acid and gamma-valerolactone (GVL) from cellulose using GVL as a solvent in biphasic systems An integrated strategy for the conversion of cellulosic biomass into γ-valerolactone Production of biofuels from cellulose and corn stover using alkylphenol solvents Heterogeneous catalytic hydrogenation of biobased levulinic and succinic acids in aqueous solutions Titania-Supported Catalysts for Levulinic Acid Hydrogenation: Influence of Support and its Impact on γ-Valerolactone Yield. Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass Reactive extraction of levulinate esters and conversion to γ-valerolactone for production of liquid fuels Benchtop micromolding of polystyrene by soft lithography A chemo-enzymatic route to synthesize (S)-γ-valerolactone from levulinic acid. Levulinic Acid Biorefineries: New Challenges for Efficient Utilization of Biomass Nickel-tungsten carbide catalysts for the production of 2,5-dimethylfuran from biomass-derived molecules. Ruthenium-catalyzed conversion of levulinic acid to pyrrolidines by reductive amination Kinetics and reaction engineering of levulinic acid production from aqueous glucose solutions. Direct Production of 5-Hydroxymethylfurfural via Catalytic Conversion of Simple and Complex Sugars over Phosphated TiO2. Decarboxylation of Lactones over Zn/ZSM-5: Elucidation of the Structure of the Active Site and Molecular Interactions. Zinc-incorporated Microporous for Mild Catalytic Hydrolysis of Gamma-valerolactone: A New Selective Route for Biomass Conversion Direct Catalytic Transformation of Biomass Derivatives into Biofuel Component γ-Valerolactone with Magnetic Nickel-Zirconium Nanoparticles Advanced Biofuels and Beyond: Chemistry Solutions for Propulsion and Production. Sequential Enzymatic Conversion of α-Angelica Lactone to γ-Valerolactone through Hydride-Independent C=C Bond Isomerization. In Situ Catalytic Hydrogenation of Biomass-Derived Methyl Levulinate to γ-Valerolactone in Methanol A Glimpse on Green Chemistry Practices in the Pharmaceutical Industry Increasing the revenue from lignocellulosic biomass: Maximizing feedstock utilization Eco-solvents--cluster-formation, surfactantless microemulsions and facilitated hydrotropy Solubility of Organosolv Lignin in γ-Valerolactone/Water Binary Mixtures. Selective Hydrogenation of Furfural to Furfuryl Alcohol in the Presence of a Recyclable Cobalt/SBA-15 Catalyst. Efficient Hydrogenation of Biomass Oxoacids to Lactones by Using NHC-Iridium Coordination Polymers as Solid Molecular Catalysts. From Diols to Lactones under Aerobic Conditions using a Laccase/TEMPO Catalytic System in Aqueous Medium Hydrodeoxygenation of the Angelica Lactone Dimer, a Cellulose-Based Feedstock: Simple, High-Yield Synthesis of Branched C7-C10Gasoline-like Hydrocarbons Selective hydrogenation of levulinic acid to γ-valerolactone over a Ru/Mg–LaO catalyst Acid-Functionalized Mesoporous Carbon: An Efficient Support for Ruthenium-Catalyzed γ-Valerolactone Production Production of 4-valerolactone by an equilibrium-limited transformation in a partitioning bioreactor: impact of absorptive polymer properties. Low-Temperature Continuous-Flow Dehydration of Xylose Over Water-Tolerant Niobia-Titania Heterogeneous Catalysts Microwave-Assisted Conversion of Levulinic Acid to γ-Valerolactone Using Low-Loaded Supported Iron Oxide Nanoparticles on Porous Silicates Interfacial acidity in ligand-modified ruthenium nanoparticles boosts the hydrogenation of levulinic acid to gamma-valerolactone High conversion of glucose to 5-hydroxymethylfurfural using hydrochloric acid as a catalyst and sodium chloride as a promoter in a water/γ-valerolactone system Sustainable Continuous Flow Valorization of γ-Valerolactone with Trioxane to α-Methylene-γ-Valerolactone over Basic Beta Zeolites Avoiding hot-spots in Microwave-assisted Pd/C catalysed reactions by using the biomass derived solvent γ-Valerolactone. Heterogeneous C–H alkenylations in continuous-flow: oxidative palladium-catalysis in a biomass-derived reaction medium

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