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Revisiting alkaline aerobic lignin oxidation

https://doi.org/10.1039/c8gc00502h
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The 99 checked references that resolve
resolves10.1021/acs.chemrev.5b00155
Catalytic Transformation of Lignin for the Production of Chemicals and Fuels
resolves10.1021/cr900354u
The Catalytic Valorization of Lignin for the Production of Renewable Chemicals
resolves10.1039/C7CS00566K
Chemicals from lignin: an interplay of lignocellulose fractionation, depolymerisation, and upgrading
resolves10.1021/acs.chemrev.7b00588
Bright Side of Lignin Depolymerization: Toward New Platform Chemicals
resolves10.1104/pp.110.155119
Lignin Biosynthesis and Structure
resolves10.1016/j.indcrop.2008.03.008
Lignin in straw of herbaceous crops
resolves10.1111/j.1469-8137.2012.04337.x
Metabolic engineering of novel lignin in biomass crops
resolves10.1007/s12155-015-9583-4
Naturally p-Hydroxybenzoylated Lignins in Palms
resolves10.1039/b411428k
Preparation and relevance of a cross-coupling product between sinapyl alcohol and sinapyl p-hydroxybenzoate
resolves10.1126/science.1246843
Lignin Valorization: Improving Lignin Processing in the Biorefinery
resolves10.1002/anie.201510351
Paving the Way for Lignin Valorisation: Recent Advances in Bioengineering, Biorefining and Catalysis
resolves10.1039/C7GC01479A
Lignin transformations for high value applications: towards targeted modifications using green chemistry
resolves10.1002/9783527699827.ch23
Catalysis in Lignocellulosic Biorefineries: The Case of Lignin Conversion
resolves10.1039/C7EE01298E
Lignin-first biomass fractionation: the advent of active stabilisation strategies
resolves10.1039/C7GC01676J
Towards high-yield lignin monomer production
resolves10.1002/9780470975831.ch10
Fundamentals of Biomass Pretreatment by Fractionation
resolves10.1146/annurev-chembioeng-061010-114205
Deconstruction of Lignocellulosic Biomass to Fuels and Chemicals
resolves10.1021/ie801542g
Methods for Pretreatment of Lignocellulosic Biomass for Efficient Hydrolysis and Biofuel Production
resolves10.1007/BF00350807
Chemistry of delignification
resolves10.1007/s12155-015-9655-5
Lignin Structural Alterations in Thermochemical Pretreatments with Limited Delignification
resolves10.1021/sc400384w
A Mechanistic Investigation of Acid-Catalyzed Cleavage of Aryl-Ether Linkages: Implications for Lignin Depolymerization in Acidic Environments
resolves10.1126/science.aaf7810
Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization
resolves10.1002/cssc.201600237
Lignin Valorization through Catalytic Lignocellulose Fractionation: A Fundamental Platform for the Future Biorefinery
resolves10.1021/acssuschemeng.6b01858
Reductive Catalytic Fractionation of Corn Stover Lignin
resolves10.1016/j.joule.2017.10.004
Flowthrough Reductive Catalytic Fractionation of Biomass
resolves10.1039/C5EE00204D
Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps
resolves10.1039/C7GC01324H
Integrating lignin valorization and bio-ethanol production: on the role of Ni-Al <sub>2</sub> O <sub>3</sub> catalyst pellets during lignin-first fractionation
resolves10.1039/C7GC02731A
Lignin depolymerization to monophenolic compounds in a flow-through system
resolves10.1021/jf060722v
Toward a Better Understanding of the Lignin Isolation Process from Wood
resolves10.1080/02773813.2014.892993
How Well Do MWL and CEL Preparations Represent the Whole Hardwood Lignin?
resolves10.1039/C5EE03718B
DMR (deacetylation and mechanical refining) processing of corn stover achieves high monomeric sugar concentrations (230 g L <sup>−1</sup> ) during enzymatic hydrolysis and high ethanol concentrations (&gt;10% v/v) during fermentation without hydrolysate purification or concentration
resolves10.1021/acssuschemeng.6b02892
Ammonia Pretreatment of Corn Stover Enables Facile Lignin Extraction
resolves10.1039/C6GC00298F
Isolation and characterization of new lignin streams derived from extractive-ammonia (EA) pretreatment
resolves10.1039/C5EE01322D
Lignin monomer production integrated into the γ-valerolactone sugar platform
resolves10.1039/C5GC01120E
Ethanol as capping agent and formaldehyde scavenger for efficient depolymerization of lignin to aromatics
resolves10.1039/C5GC01643F
Efficient catalytic hydrotreatment of Kraft lignin to alkylphenolics using supported NiW and NiMo catalysts in supercritical methanol
resolves10.1039/C7GC00195A
Phenolic acetals from lignins of varying compositions via iron( <scp>iii</scp> ) triflate catalysed depolymerisation
resolves10.1021/jacs.5b03693
Aromatic Monomers by in Situ Conversion of Reactive Intermediates in the Acid-Catalyzed Depolymerization of Lignin
resolves10.1007/978-3-642-28418-2_12
Lignin as Source of Fine Chemicals: Vanillin and Syringaldehyde
resolves10.1021/acssuschemeng.5b01344
Vanillin Production from Lignin and Its Use as a Renewable Chemical
resolves10.1039/C5GC03061G
Heterogeneous catalytic oxidation for lignin valorization into valuable chemicals: what results? What limitations? What trends?
resolves10.1002/cssc.201300964
Selective Conversion of Biorefinery Lignin into Dicarboxylic Acids
resolves10.1002/ceat.201400660
Alkaline Partial Wet Oxidation of Lignin for the Production of Carboxylic Acids
resolves10.1002/cssc.201402503
Catalytic Oxidation of Biorefinery Lignin to Value‐added Chemicals to Support Sustainable Biofuel Production
resolves10.1016/j.cherd.2010.01.021
Vanillin production from lignin oxidation in a batch reactor
resolves10.1515/hfsg.1995.49.3.273
Production of Vanillin by Oxidation of Pine Kraft Lignins with Oxygen
resolves10.1021/ie303349j
Oxidation of Lignin from<i>Eucalyptus globulus</i>Pulping Liquors to Produce Syringaldehyde and Vanillin
resolves10.1021/ie950267k
Kinetics of Vanillin Production from Kraft Lignin Oxidation
resolves10.1021/ie102132a
Insights into Oxidative Conversion of Lignin to High-Added-Value Phenolic Aldehydes
resolves10.1023/A:1005620521240
On the Role of Retroaldol Reaction in the Process of Lignin Oxidation into Vanillin. Kinetics of the Vanillideneacetone Cleavage in Alkaline Media
resolves10.1023/B:KICA.0000038087.95130.a5
New Mechanism for the Catalytic Oxidation of Lignin to Vanillin
resolves10.3390/ijms18112421
Catalytic Oxidation of Lignins into the Aromatic Aldehydes: General Process Trends and Development Prospects
resolves10.1385/ABAB:91-93:1-9:71
Production of Oxychemicals from Precipitated Hardwood Lignin
resolves10.1021/ie101402t
Kinetics of Eucalypt Lignosulfonate Oxidation to Aromatic Aldehydes by Oxygen in Alkaline Medium
resolves10.1021/ie00027a034
Improved Alkaline Oxidation Process for the Production of Aldehydes (Vanillin and Syringaldehyde) from Steam-Explosion Hardwood Lignin
resolves10.1016/j.biombioe.2017.10.046
Alkaline oxidative cracking for effective depolymerization of biorefining lignin to mono-aromatic compounds and organic acids with molecular oxygen
resolves10.1002/cssc.200800050
Oxidation of Lignin Using Aqueous Polyoxometalates in the Presence of Alcohols
resolves10.1515/hf.2011.071
Acidic oxidation of kraft lignin into aromatic monomers catalyzed by transition metal salts
resolves10.1002/adsc.200800614
The Aerobic Oxidative Cleavage of Lignin to Produce Hydroxyaromatic Benzaldehydes and Carboxylic Acids <i>via</i> Metal/Bromide Catalysts in Acetic Acid/Water Mixtures
resolves10.1002/cssc.201500131
Copper‐ and Vanadium‐Catalyzed Oxidative Cleavage of Lignin using Dioxygen
resolves10.1002/cssc.200900242
Oxidative Depolymerization of Lignin in Ionic Liquids
resolves10.1039/C5GC01950H
Lignin oxidation and depolymerisation in ionic liquids
resolves10.1021/op9900028
Fine Chemicals from Lignosulfonates. 1. Synthesis of Vanillin by Oxidation of Lignosulfonates
resolves10.1021/ie4007744
Catalytic Conversion of Sodium Lignosulfonate to Vanillin: Engineering Aspects. Part 1. Effects of Processing Conditions on Vanillin Yield and Selectivity
resolves10.1007/BF02075847
On the mechanism of vanillin formation in the catalytic oxidation of lignin with oxygen
resolves10.1007/s002260100089
Oxidation of hardwood kraft-lignin to phenolic derivatives with oxygen as oxidant
resolves10.1002/ceat.270190206
Kinetics of vanillin oxidation
resolves10.1080/02773819108050276
Reactivities of Guaiacyl and Syringyl Lignin Model Phenols Towards Oxidation with Oxygen-Alkali
resolves10.1007/BF00350692
Chemistry of delignification
resolves10.1080/02773819508009507
Catalytic Mechanism of Cu<sup>2+</sup>and Fe<sup>3+</sup>in Alkaline O<sub>2</sub>Oxidation of Lignin
resolves10.1021/ie0601697
Kinetic Evaluation and Modeling of Lignin Catalytic Wet Oxidation to Selective Production of Aromatic Aldehydes
resolves10.1021/ef100768e
Catalysis of Cu-Doped Co-Based Perovskite-Type Oxide in Wet Oxidation of Lignin To Produce Aromatic Aldehydes
resolves10.1021/ef8005349
Activity and Stability of Perovskite-Type Oxide LaCoO<sub>3</sub>Catalyst in Lignin Catalytic Wet Oxidation to Aromatic Aldehydes Process
resolves10.1007/s10562-008-9588-0
Perovskite-type Oxide LaMnO3: An Efficient and Recyclable Heterogeneous Catalyst for the Wet Aerobic Oxidation of Lignin to Aromatic Aldehydes
resolves10.3390/molecules14082747
Wet Aerobic Oxidation of Lignin into Aromatic Aldehydes Catalysed by a Perovskite-type Oxide: LaFe1-xCuxO3 (x=0, 0.1, 0.2)
resolves10.1016/j.apcata.2008.01.006
Reaction kinetics of liquid phase air oxidation of p-cresol to p-hydroxybenzaldehyde
resolves10.1016/j.apcata.2014.08.023
Effect of preparation parameters on characterization and activity of Co3O4 catalyst in liquid phase oxidation of lignin model substrates
resolves10.1080/02773819708003131
Oxidation of Hardwood Kraft-Lignin to Phenolic Derivatives. Nitrobenzene and Copper Oxide as Oxidants
resolves10.1139/v67-487
Lignin oxidation. Preferential use of cupric oxide
resolves10.1021/cs500606g
Perovskite Oxides: Preparation, Characterizations, and Applications in Heterogeneous Catalysis
resolves10.1021/cr500032a
Perovskites as Substitutes of Noble Metals for Heterogeneous Catalysis: Dream or Reality
resolves10.1016/S0926-3373(00)00215-0
AFeO3 (A=La, Nd, Sm) and LaFe1−xMgxO3 perovskites as methane combustion and CO oxidation catalysts: structural, redox and catalytic properties
resolves10.1006/jssc.1999.8327
Perovskite-Type Oxides
resolves10.1016/S0040-6031(00)00532-3
Oxygen non-stoichiometry and reducibility of B-site substituted lanthanum manganites
resolves10.1016/0021-9517(81)90171-8
The surface chemistry of some perovskite oxides
resolves10.1046/j.1365-313x.2000.00727.x
Modified lignin in tobacco and poplar plants over‐expressing the Arabidopsis gene encoding ferulate 5‐hydroxylase
resolves10.1385/1-59745-131-2:143
Poplar (Populus spp.)
resolves10.1016/j.copbio.2015.10.009
Designer lignins: harnessing the plasticity of lignification
resolves10.1002/cssc.201600648
Hydrogen‐free catalytic fractionation of woody biomass
resolves10.1039/C7GC03747C
<i>In situ</i> recovery of bio-based carboxylic acids
resolves10.1039/C4EE03230F
Adipic acid production from lignin
resolves10.1021/acscatal.5b02906
Influence of Acidic (H<sub>3</sub>PO<sub>4</sub>) and Alkaline (NaOH) Additives on the Catalytic Reductive Fractionation of Lignocellulose
resolves10.1039/C7GC03110F
Mechanistic studies of base-catalysed lignin depolymerisation in dimethyl carbonate
resolves10.1080/15422119.2015.1070178
Recovery of Vanillin and Syringaldehyde from Lignin Oxidation: A Review of Separation and Purification Processes
resolves10.1021/acssuschemeng.5b01451
Base-Catalyzed Depolymerization of Biorefinery Lignins
resolves10.1039/B916070A
Solution-state 2D NMR of ball-milled plant cell wall gels in DMSO-d6/pyridine-d5
resolves10.1038/nprot.2012.064
Whole plant cell wall characterization using solution-state 2D NMR
resolves10.1039/C5EE03051J
Next-generation ammonia pretreatment enhances cellulosic biofuel production
The 3 references without a DOI — listed, not checked
no DOI — not checkedJ. Lora , in Monomers, Polymers and Composites from Renewable Resources , ed. M. N. B. Gandini and M. N. Belgacem , Elsevier , Amsterdam , 2008 , pp. 225–241
no DOI — not checkedR. Davis , L.Tao , E.Tan , M.Biddy , G.Beckham , C.Scarlata , J.Jacobson , K.Cafferty , J.Ross and J.Lukas
no DOI — not checkedC8GC00502H-(cit54)/*[position()=1]
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