Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
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Solvents and sustainable chemistryReactions of Cl atoms with alkyl esters: kinetic, mechanism and atmospheric implications.Increasing the revenue from lignocellulosic biomass: Maximizing feedstock utilizationHydrodeoxygenation of the angelica lactone dimer, a cellulose-based feedstock: simple, high-yield synthesis of branched C7 -C10 gasoline-like hydrocarbons.High performing and stable supported nano-alloys for the catalytic hydrogenation of levulinic acid to γ-valerolactoneDecarboxylation of Lactones over Zn/ZSM-5: Elucidation of the Structure of the Active Site and Molecular Interactions.Bio-based solvents: an emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry.State of the art of Lewis acid-containing zeolites: lessons from fine chemistry to new biomass transformation processes.Redefining biorefinery: the search for unconventional building blocks for materials.Chemical Conversions of Biomass-Derived Platform Chemicals over Copper-Silica Nanocomposite Catalysts.Selective Conversion of 5-Hydroxymethylfuraldehyde Using Cp*Ir Catalysts in Aqueous Formate Buffer Solution.Organocatalytic upgrading of furfural and 5-hydroxymethyl furfural to C10 and C12 furoins with quantitative yield and atom-efficiency.Expanding the biomass derived chemical space.Domino reaction catalyzed by zeolites with Brønsted and Lewis acid sites for the production of γ-valerolactone from furfural.Influence of Levulinic Acid Hydrogenation on Aluminum Coordination in Zeolite-Supported Ruthenium Catalysts: A (27) Al 3QMAS Nuclear Magnetic Resonance Study.New Insights into the Reactivity of Biomass with Butenes for the Synthesis of Butyl Levulinates.Catalytic Conversion of Carbohydrates to Levulinate Ester over Heteropolyanion-Based Ionic Liquids.Microwave-Assisted γ-Valerolactone Production for Biomass Lignin Extraction: A Cascade Protocol.A metabolic pathway for catabolizing levulinic acid in bacteria.Conversion of levulinic acid into γ-valerolactone using Fe3(CO)12: mimicking a biorefinery setting by exploiting crude liquors from biomass acid hydrolysis.Advanced biorefinery based on the fractionation of biomass in γ-valerolactone and water.Biosourced polymetallic catalysts: an efficient means to synthesize underexploited platform molecules from carbohydrates.New Sustainable Model of Biorefineries: Biofactories and Challenges of Integrating Bio- and Solar Refineries.Introducing Glycerol as a Sustainable Solvent to Organolithium Chemistry: Ultrafast Chemoselective Addition of Aryllithium Reagents to Nitriles under Air and at Ambient Temperature.New catalytic strategies for α,ω-diols production from lignocellulosic biomass.Angelica Lactones: From Biomass-Derived Platform Chemicals to Value-Added Products.Solubility of Organosolv Lignin in γ-Valerolactone/Water Binary Mixtures.Synthesis of 2,2-bis(pyridin-2-yl amino)cyclobutanols and their conversion into 5-(pyridin-2-ylamino)dihydrofuran-2(3H)-ones.Recyclable Earth-Abundant Metal Nanoparticle Catalysts for Selective Transfer Hydrogenation of Levulinic Acid to Produce γ-Valerolactone.Titania-Supported Catalysts for Levulinic Acid Hydrogenation: Influence of Support and its Impact on γ-Valerolactone Yield.Direct Production of 5-Hydroxymethylfurfural via Catalytic Conversion of Simple and Complex Sugars over Phosphated TiO2.Catalyst characterization in the presence of solvent: development of liquid phase structure-activity relationships.An integrated strategy for the conversion of cellulosic biomass into γ-valerolactoneHydrodeoxygenation of the Angelica Lactone Dimer, a Cellulose-Based Feedstock: Simple, High-Yield Synthesis of Branched C7-C10Gasoline-like HydrocarbonsHigh conversion of glucose to 5-hydroxymethylfurfural using hydrochloric acid as a catalyst and sodium chloride as a promoter in a water/γ-valerolactone systemA PDMS membrane with high pervaporation performance for the separation of furfural and its potential in industrial applicationCompositional and structural feedstock requirements of a liquid phase cellulose-to-naphtha process in a carbon- and hydrogen-neutral biorefinery contextInterfacial acidity in ligand-modified ruthenium nanoparticles boosts the hydrogenation of levulinic acid to gamma-valerolactoneRuthenium(ii) oxidase catalysis for C–H alkenylations in biomass-derived γ-valerolactoneCatalytic, Enantioselective Vinylogous Mukaiyama Aldol Reaction of Furan-Based Dienoxy Silanes: A Chemodivergent Approach to γ-Valerolactone Flavan-3-ol Metabolites and δ-Lactone Analogues
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Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
description
im Jahr 2013 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2013
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name
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
@en
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
@nl
type
label
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
@en
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
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prefLabel
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
@en
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
@nl
P2860
P356
P1433
P1476
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
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P2093
Stephanie G. Wettstein
P2860
P356
10.1039/C3GC37065H
P407
P577
2013-01-01T00:00:00Z