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Catalytic Conversion of Biomass to Furanic Derivatives with Deep Eutectic Solvents
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The 127 checked references that resolve
resolves10.1039/C7GC02145C
Isomerization of glucose to fructose catalyzed by lithium bromide in water
resolves10.1039/c2ee23440h
Food waste as a valuable resource for the production of chemicals, materials and fuels. Current situation and global perspective
resolves10.1016/j.bej.2015.12.016
Valorization of organic residues for the production of added value chemicals: A contribution to the bio-based economy
resolves10.1021/acssuschemeng.8b01271
Biocompatible Choline-Based Deep Eutectic Solvents Enable One-Pot Production of Cellulosic Ethanol
resolves10.1039/b922014c
Technology development for the production of biobased products from biorefinery carbohydrates—the US Department of Energy’s “Top 10” revisited
resolves10.1016/j.apcatb.2018.01.006
Nitrogen-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.molcata.2016.11.023
Synergism studies on alumina-supported copper-nickel catalysts towards furfural and 5-hydroxymethylfurfural hydrogenation
resolves10.1039/C9GC03856F
Selective hydrogenation of 5-hydroxymethylfurfural and its acetal with 1,3-propanediol to 2,5-bis(hydroxymethyl)furan using supported rhenium-promoted nickel catalysts in water
resolves10.1186/s42500-020-00012-5
Recent progress in the development of advanced biofuel 5-ethoxymethylfurfural
resolves10.1039/C8GC02680G
Production of 2,5-furandicarboxylic acid (FDCA) from 5-hydroxymethylfurfural (HMF): recent progress focusing on the chemical-catalytic routes
resolves10.1016/j.rser.2017.02.042
Recent advances in catalytic transformation of biomass-derived 5-hydroxymethylfurfural into the innovative fuels and chemicals
resolves10.1021/acscatal.7b03530
Catalytic Advances in the Production and Application of Biomass-Derived 2,5-Dihydroxymethylfuran
resolves10.1021/cs5012926
Selective Hydrogenation of Biomass-Based 5-Hydroxymethylfurfural over Catalyst of Palladium Immobilized on Amine-Functionalized Metal–Organic Frameworks
resolves10.1007/s10562-011-0581-7
Hydrodeoxygenation of Furfural Over Supported Metal Catalysts: A Comparative Study of Cu, Pd and Ni
resolves10.1016/j.chempr.2018.07.007
Toward an Integrated Conversion of 5-Hydroxymethylfurfural and Ethylene for the Production of Renewable p-Xylene
resolves10.1039/D0GC00208A
Haber-independent, diversity-oriented synthesis of nitrogen compounds from biorenewable chitin
resolves10.1007/s10570-020-03411-3
Homogenous hydrolysis of cellulose to glucose in an inorganic ionic liquid catalyzed by zeolites
resolves10.1039/C6RA25025D
Effective conversion of biomass into bromomethylfurfural, furfural, and depolymerized lignin in lithium bromide molten salt hydrate of a biphasic system
resolves10.1021/cr300182k
Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources
resolves10.1016/j.rser.2015.12.315
Thermochemical conversion of triglycerides for production of drop-in liquid fuels
resolves10.1016/j.rser.2018.12.010
Recent advances in catalytic conversion of biomass to 5-hydroxymethylfurfural and 2, 5-dimethylfuran
resolves10.1039/C7CS00213K
Catalytic oxidation of carbohydrates into organic acids and furan chemicals
resolves10.1021/ja0351802
Controlling the Aqueous Miscibility of Ionic Liquids: Aqueous Biphasic Systems of Water-Miscible Ionic Liquids and Water-Structuring Salts for Recycle, Metathesis, and Separations
resolves10.1126/science.1141199
Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural
resolves10.1002/cssc.201000184
Hydrolysis of Cellulose by Using Catalytic Amounts of FeCl<sub>2</sub> in Ionic Liquids
resolves10.1002/cssc.201702016
Acid‐Catalyzed Conversion of Carbohydrates into Value‐Added Small Molecules in Aqueous Media and Ionic Liquids
resolves10.1021/acs.chemrev.6b00457
Catalytic Transformation of Lignocellulose into Chemicals and Fuel Products in Ionic Liquids
resolves10.1039/C9GC00704K
Short-time deep eutectic solvent pretreatment for enhanced enzymatic saccharification and lignin valorization
resolves10.1039/b419172b
Toxicity and antimicrobial activity of imidazolium and pyridinium ionic liquids
resolves10.1021/ja048266j
Deep Eutectic Solvents Formed between Choline Chloride and Carboxylic Acids: Versatile Alternatives to Ionic Liquids
resolves10.1021/je060038c
Solubility of Metal Oxides in Deep Eutectic Solvents Based on Choline Chloride
resolves10.1016/j.biotechadv.2018.08.009
Natural deep eutectic solvents for lignocellulosic biomass pretreatment: Recent developments, challenges and novel opportunities
resolves10.1016/j.biortech.2018.06.027
Integration of facile deep eutectic solvents pretreatment for enhanced enzymatic hydrolysis and lignin valorization from industrial xylose residue
resolves10.1002/anie.201207548
Low‐Transition‐Temperature Mixtures (LTTMs): A New Generation of Designer Solvents
resolves10.1002/ange.201207548
Mischungen mit niedriger Übergangstemperatur (LTTMs) – eine neue Generation von Designer‐Lösungsmitteln
resolves10.1021/jacs.9b12117
Binding Energy as Driving Force for Controllable Reconstruction of Hydrogen Bonds with Molecular Scissors
resolves10.1002/cctc.201500134
Contribution of Deep Eutectic Solvents for Biomass Processing: Opportunities, Challenges, and Limitations
resolves10.1039/b210714g
Novel solvent properties of choline chloride/urea mixturesElectronic supplementary information (ESI) available: spectroscopic data. See http://www.rsc.org/suppdata/cc/b2/b210714g/
resolves10.1039/D0GC02439B
Structure–function relationships of deep eutectic solvents for lignin extraction and chemical transformation
resolves10.1002/cssc.201700457
Green Processing of Lignocellulosic Biomass and Its Derivatives in Deep Eutectic Solvents
resolves10.1016/j.gee.2019.01.012
Application of deep eutectic solvents in biomass pretreatment and conversion
resolves10.1039/C8GC03064B
Facile fractionation of lignocelluloses by biomass-derived deep eutectic solvent (DES) pretreatment for cellulose enzymatic hydrolysis and lignin valorization
resolves10.1002/cssc.201601795
Efficient Cleavage of Lignin–Carbohydrate Complexes and Ultrafast Extraction of Lignin Oligomers from Wood Biomass by Microwave‐Assisted Treatment with Deep Eutectic Solvent
resolves10.1002/cssc.201900147
Quest for Green‐Solvent Design: From Hydrophilic to Hydrophobic (Deep) Eutectic Solvents
resolves10.1039/C4RA05049E
Simultaneous dehydration of biomass-derived sugars to 5-hydroxymethyl furfural (HMF) and reduction of graphene oxide in ethyl lactate: one pot dual chemistry
resolves10.1039/c2gc35660k
New natural and renewable low transition temperature mixtures (LTTMs): screening as solvents for lignocellulosic biomass processing
resolves10.1016/j.cclet.2013.09.004
Synthesis and characterization of novel ternary deep eutectic solvents
resolves10.1016/j.molliq.2017.05.084
Novel low viscous, green and amphiphilic N -oxides/phenylacetic acid based Deep Eutectic Solvents
resolves10.1039/C9CC04846D
Phenolic hydrogen bond donors in the formation of non-ionic deep eutectic solvents: the quest for type V DES
resolves10.1007/s10570-018-2130-7
Deep eutectic solvents (DESs) for cellulose dissolution: a mini-review
resolves10.1007/s10570-017-1358-y
Potential use of deep eutectic solvents to facilitate lignocellulosic biomass utilization and conversion
resolves10.1016/j.carbpol.2018.07.078
Deep eutectic solvents for polysaccharides processing. A review
resolves10.3390/catal7070218
Catalytic Conversion of Carbohydrates to Furanic Derivatives in the Presence of Choline Chloride
resolves10.1016/j.biortech.2017.09.159
Deep eutectic solvents from hemicellulose-derived acids for the cellulosic ethanol refining of Akebia’ herbal residues
resolves10.1039/b810392e
Conversion of fructose to 5-hydroxymethylfurfural using ionic liquids prepared from renewable materials
resolves10.1039/b822328a
Direct conversion of inulin to 5-hydroxymethylfurfural in biorenewable ionic liquids
resolves10.1039/C8GC04022B
Deep eutectic solvent (DES) as both solvent and catalyst for oxidation of furfural to maleic acid and fumaric acid
resolves10.1016/j.renene.2017.10.083
Conversion of sunflower stalk based cellulose to the valuable products using choline chloride based deep eutectic solvents
resolves10.1039/b917548m
Conversion of carbohydrates into 5-hydroxymethylfurfural in highly concentrated low melting mixtures
resolves10.1039/C6RA00267F
Green catalytic conversion of bio-based sugars to 5-chloromethyl furfural in deep eutectic solvent, catalyzed by metal chlorides
resolves10.1002/jctb.5312
An effective pathway for 5‐brominemethylfurfural synthesis from biomass sugars in deep eutectic solvent
resolves10.1039/C8CC03798A
Catalytic deep eutectic solvents for highly efficient conversion of cellulose to gluconic acid with gluconic acid self-precipitation separation
resolves10.1016/j.jiec.2019.08.057
Synthesis of renewable monomer 2, 5-bishydroxymethylfuran from highly concentrated 5-hydroxymethylfurfural in deep eutectic solvents
resolves10.1021/acssuschemeng.8b01788
Deep Eutectic Solvents: Green Solvents and Catalysts for the Preparation of Pyrazine Derivatives by Self-Condensation of <scp>d</scp>-Glucosamine
resolves10.1021/acssuschemeng.6b00882
Alcohol Effect and the Related Mechanism on Fructose Dehydration into 5-Hydroxymethylfurfural in the Deep Eutectic Solvent of [Emim]Cl/Alcohol
resolves10.1039/B918922J
High-yield conversion of plant biomass into the key value-added feedstocks 5-(hydroxymethyl)furfural, levulinic acid, and levulinic esters via5-(chloromethyl)furfural
resolves10.1002/cssc.200900136
Dramatic Advancements in the Saccharide to 5‐(Chloromethyl)furfural Conversion Reaction
resolves10.1016/j.biortech.2015.05.053
Deep eutectic solvent pretreatment and subsequent saccharification of corncob
resolves10.1016/j.biortech.2018.05.016
Pretreatment of wheat straw using basic ethanolamine-based deep eutectic solvents for improving enzymatic hydrolysis
resolves10.1016/j.biortech.2017.10.019
Insight into the structure-function relationships of deep eutectic solvents during rice straw pretreatment
resolves10.3390/molecules23081891
Biorenewable Deep Eutectic Solvent for Selective and Scalable Conversion of Furfural into Cyclopentenone Derivatives
resolves10.1016/j.molliq.2013.11.036
Room temperature ionic liquid choline chloride–oxalic acid: A versatile catalyst for acid-catalyzed transformation in organic reactions
resolves10.1016/j.tetlet.2015.12.014
Choline chloride/urea as a deep eutectic solvent/organocatalyst promoted three-component synthesis of 3-aminoimidazo-fused heterocycles via Groebke–Blackburn–Bienayme process
resolves10.1016/j.crci.2017.01.008
Solvent-catalyzed umpolung carbonsulfur bond-forming reactions by nucleophilic addition of thiolate and sulfinate ions to in situ–derived nitrosoalkenes in deep eutectic solvents
resolves10.3390/molecules21070924
An Expeditious and Greener Synthesis of 2-Aminoimidazoles in Deep Eutectic Solvents
resolves10.1016/j.cej.2019.123580
Continuous synthesis of 5-hydroxymethylfurfural using deep eutectic solvents and its kinetic study in microreactors
resolves10.1002/cssc.201100489
The Production of 5‐Hydroxymethylfurfural from Fructose in Isopropyl Alcohol: A Green and Efficient System
resolves10.1021/sc5004659
Acid-Catalyzed Conversion of Xylose in 20 Solvents: Insight into Interactions of the Solvents with Xylose, Furfural, and the Acid Catalyst
resolves10.1002/jctb.5954
Biological oxidation of choline‐based ionic liquids in sequencing batch reactors
resolves10.1002/cssc.201802342
Development of Betaine‐Based Sustainable Catalysts for Green Conversion of Carbohydrates and Biomass into 5‐Hydroxymethylfurfural
resolves10.1016/j.renene.2020.09.019
Effective selectivity conversion of glucose to furan chemicals in the aqueous deep eutectic solvent
resolves10.1039/b800045j
Flexible coordination environments of lanthanide complexes grown from chloride-based ionic liquids
resolves10.1016/j.biortech.2009.09.010
Microwave-assisted conversion of lignocellulosic biomass into furans in ionic liquid
resolves10.1039/C1GC16236E
Conversion of fructose and inulin to 5-hydroxymethylfurfural in sustainable betaine hydrochloride-based media
resolves10.1007/s10570-017-1465-9
Production of cellulose carbamate using urea-based deep eutectic solvents
resolves10.1016/j.biombioe.2014.11.001
Conversion of glucose into 5-hydroxymethylfurfural with boric acid in molten mixtures of choline salts and carboxylic acids
resolves10.1016/j.indcrop.2017.01.027
Green process for production of 5-hydroxymethylfurfural from carbohydrates with high purity in deep eutectic solvents
resolves10.1002/cssc.201200186
Dehydration of Highly Concentrated Solutions of Fructose to 5‐Hydroxymethylfurfural in a Cheap and Sustainable Choline Chloride/Carbon Dioxide System
resolves10.15376/biores.8.4.6014-6025
Conversion of Xylan and Xylose into Furfural in Biorenewable Deep Eutectic Solvent with Trivalent Metal Chloride Added
resolves10.1016/j.cclet.2014.03.029
Conversion of xylose and xylan into furfural in biorenewable choline chloride–oxalic acid deep eutectic solvent with the addition of metal chloride
resolves10.1039/C4RA10121A
Conversion of highly concentrated fructose into 5-hydroxymethylfurfural by acid–base bifunctional HPA nanocatalysts induced by choline chloride
resolves10.1016/j.fuel.2015.10.014
Lysine functional heteropolyacid nanospheres as bifunctional acid–base catalysts for cascade conversion of glucose to levulinic acid
resolves10.1039/C5GC01336D
A choline chloride/DMSO solvent for the direct synthesis of diformylfuran from carbohydrates in the presence of heteropolyacids
resolves10.1002/cssc.201402761
Catalytic Dehydration of Carbohydrates Suspended in Organic Solvents Promoted by AlCl<sub>3</sub>/SiO<sub>2</sub> Coated with Choline Chloride
resolves10.1016/j.fuel.2019.02.112
A highly selective and efficient method for the production of 5-hydroxymethylfurfural from dehydration of fructose using SACS/DES catalytic system
resolves10.1016/j.indcrop.2017.11.001
An effective pathway for converting carbohydrates to biofuel 5-ethoxymethylfurfural via 5-hydroxymethylfurfural with deep eutectic solvents (DESs)
resolves10.1021/acssuschemeng.9b02605
Activity of a Heterogeneous Catalyst in Deep Eutectic Solvents: The Case of Carbohydrate Conversion into 5-Hydroxymethylfurfural
resolves10.1002/ange.201602883
Critical Influence of 5‐Hydroxymethylfurfural Aging and Decomposition on the Utility of Biomass Conversion in Organic Synthesis
resolves10.1002/cssc.201802792
Synthesis of MCM‐41‐Supported Metal Catalysts in Deep Eutectic Solvent for the Conversion of Carbohydrates into 5‐Hydroxymethylfurfural
resolves10.1021/acssuschemeng.6b00485
Are Aqueous Biphasic Systems Composed of Deep Eutectic Solvents Ternary or Quaternary Systems?
resolves10.1016/j.fuel.2014.09.102
One-pot production of a liquid biofuel candidate—Ethyl levulinate from glucose and furfural residues using a combination of extremely low sulfuric acid and zeolite USY
resolves10.1002/apj.2095
One‐pot ethanolysis of carbohydrates to promising biofuels: 5‐ethoxymethylfurfural and ethyl levulinate
resolves10.1021/acs.energyfuels.9b00357
Efficient One-Pot Production of Biofuel 5-Ethoxymethylfurfural from Corn Stover: Optimization and Kinetics
resolves10.1007/s11814-018-0025-9
Efficient conversion of fructose to 5-[(formyloxy)methyl]furfural by reactive extraction and in-situ esterification
resolves10.1039/c1gc15550d
Microwave assisted conversion of carbohydrates and biopolymers to 5-hydroxymethylfurfural with aluminium chloride catalyst in water
resolves10.1021/je700638u
Solubility of CO
<sub>2</sub>
in a Choline Chloride + Urea Eutectic Mixture
resolves10.3390/catal7060182
Insights into the Metal Salt Catalyzed 5-Ethoxymethylfurfural Synthesis from Carbohydrates
resolves10.1016/j.fuel.2013.06.015
Efficient conversion of carbohydrates into 5-ethoxymethylfurfural in ethanol catalyzed by AlCl3
resolves10.1039/c3gc41495g
Selectivity enhancement in the aqueous acid-catalyzed conversion of glucose to 5-hydroxymethylfurfural induced by choline chloride
resolves10.1080/01614940.2017.1321452
Supported solid and heteropoly acid catalysts for production of biodiesel
resolves10.1002/cssc.202000537
Oxidative Esterification of 5‐Hydroxymethylfurfural with an N‐doped Carbon‐supported CoCu Bimetallic Catalyst
resolves10.1016/j.indcrop.2018.12.027
Efficient conversion of corn stover into 5-ethoxymethylfurfural catalyzed by zeolite USY in ethanol/THF medium
resolves10.1002/cssc.201200363
Acid‐Catalyzed Dehydration of Fructose into 5‐Hydroxymethylfurfural by Cellulose‐Derived Amorphous Carbon
resolves10.1039/C4RA15296D
Carbonaceous microspheres prepared by hydrothermal carbonization of glucose for direct use in catalytic dehydration of fructose
resolves10.1016/j.cep.2019.03.001
Synthesis of 5-hydroxymethylfurfural (5-HMF) from fructose over cation exchange resin in a continuous flow reactor
resolves10.1007/s10570-011-9568-1
Catalytic conversion of cellulose into 5-hydroxymethylfurfural in high yields via a two-step process
resolves10.1021/ie801016s
Selective Conversion of <scp>D</scp>-Fructose to 5-Hydroxymethylfurfural by Ion-Exchange Resin in Acetone/Dimethyl sulfoxide Solvent Mixtures
resolves10.1016/S1566-7367(03)00133-X
Dehydration of fructose into 5-hydroxymethylfurfural in the presence of ionic liquids
resolves10.1021/acscatal.0c01328
Highly Selective Cross-Etherification of 5-Hydroxymethylfurfural with Ethanol
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