Ensuring the sustainability of biocatalysis
10.1002/cssc.202102683 · doi-reference
A highly efficient, selective and stable PtCoNi/MWCNTs nanocatalyst for furfural hydrogenation to furfuryl alcohol under mild reaction conditions
10.1016/j.fuel.2022.126222 · doi-reference
Co decorated low Pt loading nanoparticles over TiO2 catalyst for selective hydrogenation of furfural
10.1016/j.apcata.2022.118766 · doi-reference
Catalytic transfer hydrogenation of biomass-derived furfural into furfuryl alcohol over zirconium doped nanofiber
10.1016/j.fuel.2022.125792 · doi-reference
Optimization of Ruthenium based catalysts for the aqueous phase hydrogenation of furfural to furfuryl alcohol
10.1016/j.apcata.2018.07.010 · doi-reference
Insight into the Co2+/Co3+ sites for the selective reduction of furfural to furfuryl alcohol
10.1016/j.fuel.2022.126137 · doi-reference
Pd–Cu/SiO2 catalyzed efficient hydrogen transfer of cyclohexanol and furfural platforms into cyclohexanone and furfuryl alcohol
10.1016/j.fuel.2024.131278 · doi-reference
Biocatalytic transformation of furfural into furfuryl alcohol using resting cells of Bacillus cereus
10.1016/j.cattod.2021.01.011 · doi-reference
One-pot chemoenzymatic access to a cefuroxime precursor via C1 extension of furfural
10.1039/d4cc06522k · doi-reference
Biocatalysis making waves in organic chemistry
10.1039/d1cs00100k · doi-reference
Recent advances in the conversion of furfural into bio-chemicals through chemo- and bio-catalysis
10.1039/d1ra04633k · doi-reference
The effect of water upon deep eutectic solvent nanostructure: An unusual transition from ionic mixture to aqueous solution
10.1002/anie.201702486 · doi-reference
The acidity values of ternary DES-like mixtures based on choline chloride, lactic acid, and dihydric alcohols
10.1016/j.molliq.2023.122846 · doi-reference
10.3390/su17219492
10.3390/su17219492 · doi-reference
Deep eutectic solvents and their applications as green solvents
10.1016/j.cogsc.2019.09.004 · doi-reference
Novel ternary based natural deep eutectic solvents (NADES) for sustainable extraction of lignin nanoparticles from waste Pinus roxburghii needles: A green approach
10.1016/j.scp.2024.101518 · doi-reference
A new surfactant-based hydrophobic deep eutectic solvent for microextraction and spectrophotometric determination of Rhodamine B and Allura red in real samples
10.1016/j.microc.2025.114273 · doi-reference
10.3390/app14177662
10.3390/app14177662 · doi-reference
10.3390/chemengineering9040084
10.3390/chemengineering9040084 · doi-reference
Co-production of 2,5-dihydroxymethylfuran and furfuralcohol from sugarcane bagasse via chemobiocatalytic approach in a sustainable system
10.1016/j.biortech.2023.129819 · doi-reference
Enhanced upgrading of corncob to furfuryl alcohol with a novel silica-supported SO42—TiO2 chemocatalyst and immobilized whole-cell biocatalyst
10.1039/d3gc01764h · doi-reference
One-pot two-stage biocatalytic upgrading of biomass-derived aldehydes to optically active β-amino alcohols via sequential hydroxymethylation and asymmetric reduction amination
10.1039/d3gc04287a · doi-reference
Improved conversion of bamboo shoot shells to furfuryl alcohol and furfurylamine by a sequential catalysis with sulfonated graphite and biocatalysts
10.1039/d0ra07372e · doi-reference
Efficient production of hydroxymethyl-2-furfurylamine by chemoenzymatic cascade catalysis of bread waste in a sustainable approach
10.1016/j.biortech.2023.129454 · doi-reference
Significantly enhanced bioconversion of high titer biomass-derived furfural to furfuryl alcohol by robust endogenous aldehyde reductase in a sustainable way
10.1039/d3gc01417g · doi-reference
Effect of metal ions on the activity of ten NAD-dependent formate dehydrogenases
10.1007/s10930-020-09924-x · doi-reference
Synthesis of 5-hydroxymethyl-2-furfurylamine from bread waste via two-step reaction
10.1021/acssuschemeng.3c04032 · doi-reference
Asymmetric whole-cell bioreduction of sterically bulky 2-benzoylpyridine derivatives in aqueous hydrophilic ionic liquid media
10.1016/j.cej.2017.02.028 · doi-reference
Improved synthesis of furfurylamine from a high titer of biomass-derived furfural by a thermostable triple mutant ω-transaminase in a three-component deep eutectic solvent ChCl/Lactic acid/Malonic acid system
10.1021/acssuschemeng.3c00671 · doi-reference
10.3390/catal13010037
10.3390/catal13010037 · doi-reference
10.3390/catal11070781
10.3390/catal11070781 · doi-reference
Biological synthesis of 2,5-bis(hydroxymethyl)furan from biomass-derived 5-hydroxymethylfurfural by E. coli CCZU-K14 whole cells
10.1016/j.biortech.2017.09.071 · doi-reference
Efficient 5-hydroxymethylfurfural production in ChCl-based deep eutectic solvents using boric acid and metal chlorides
10.1039/d5ra00020c · doi-reference
Deep eutectic solvents as reusable catalysts and promoter for the greener syntheses of small molecules: Recent advances
10.1016/j.molliq.2022.121013 · doi-reference
Deep eutectic solvents for synthesis of 5-hydroxymethylfurfural
10.1016/j.cogsc.2024.100924 · doi-reference
pH-controlled efficient conversion of hemicellulose to furfural using choline—Based deep eutectic solvents as catalysts
10.1002/cssc.202101130 · doi-reference
Mechanistic investigation into the formation of humins in acid-catalyzed biomass reactions
10.1021/acsomega.2c04783 · doi-reference
Production of furfural: From kinetics to process assessment
10.1016/j.fuel.2024.133423 · doi-reference
Formation of humins during degradation of carbohydrates and furfural derivatives in various solvents
10.1007/s13399-019-00414-4 · doi-reference
Microwave mediated enhanced production of 5-hydroxymethylfurfural using choline chloride-based eutectic mixture as sustainable catalyst
10.1016/j.renene.2021.05.157 · doi-reference
