Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 90 checked references that resolve
resolves10.1039/c1cs15124jCatalytic conversion of lignocellulosic biomass to fine chemicals and fuels
resolves10.1039/c7cs00566kChemicals from lignin: an interplay of lignocellulose fractionation, depolymerisation, and upgrading
resolves10.1039/c4cs00235kLignin depolymerisation strategies: towards valuable chemicals and fuels
resolves10.1002/anie.201510351Paving the Way for Lignin Valorisation: Recent Advances in Bioengineering, Biorefining and Catalysis
resolves10.1021/cr900354uThe Catalytic Valorization of Lignin for the Production of Renewable Chemicals
resolves10.1002/cctc.201700473On the Meaning and Origins of Lignin Recalcitrance: A Critical Analysis of the Catalytic Upgrading of Lignins Obtained from Mechanocatalytic Biorefining and Organosolv Pulping
resolves10.1039/c5gc03043aNew insights into the structure and composition of technical lignins: a comparative characterisation study
resolves10.1016/j.fuel.2015.12.051High-yield and high-calorific bio-oil production from concentrated sulfuric acid hydrolysis lignin in supercritical ethanol
resolves10.1016/j.cej.2017.02.045Depolymerization of concentrated sulfuric acid hydrolysis lignin to high-yield aromatic monomers in basic sub- and supercritical fluids
resolves10.1039/c8gc02460jSolvothermal liquefaction of alkali lignin to obtain a high yield of aromatic monomers while suppressing solvent consumption
resolves10.1016/j.cej.2018.05.036A two-step approach for producing oxygen-free aromatics from lignin using formic acid as a hydrogen source
resolves10.1039/c7ee01298eLignin-first biomass fractionation: the advent of active stabilisation strategies
resolves10.1039/c5ee00204dReductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps
resolves10.1039/c8gc01031eCatalytic lignocellulose biorefining in
<i>n</i>
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resolves10.1039/c5cc04025fTuning the lignin oil OH-content with Ru and Pd catalysts during lignin hydrogenolysis on birch wood
resolves10.1002/cssc.201402017Selective Route to 2‐Propenyl Aryls Directly from Wood by a Tandem Organosolv and Palladium‐Catalysed Transfer Hydrogenolysis
resolves10.1039/c5gc01442eInfluence of bio-based solvents on the catalytic reductive fractionation of birch wood
resolves10.1021/acscatal.5b02906Influence of Acidic (H<sub>3</sub>PO<sub>4</sub>) and Alkaline (NaOH) Additives on the Catalytic Reductive Fractionation of Lignocellulose
resolves10.1002/cssc.201601252Effective Release of Lignin Fragments from Lignocellulose by Lewis Acid Metal Triflates in the Lignin‐First Approach
resolves10.1039/c6gc02962kReductive fractionation of woody biomass into lignin monomers and cellulose by tandem metal triflate and Pd/C catalysis
resolves10.1039/c4gc01911cA synergistic biorefinery based on catalytic conversion of lignin prior to cellulose starting from lignocellulosic biomass
resolves10.1039/c5gc01325aMechanistic investigation of the Zn/Pd/C catalyzed cleavage and hydrodeoxygenation of lignin
resolves10.1039/c2ee23741eLignin depolymerization (LDP) in alcohol over nickel-based catalysts via a fragmentation–hydrogenolysis process
resolves10.1002/cssc.201601273High Yield Production of Natural Phenolic Alcohols from Woody Biomass Using a Nickel‐Based Catalyst
resolves10.1002/anie.201403747Catalytic Biorefining of Plant Biomass to Non‐Pyrolytic Lignin Bio‐Oil and Carbohydrates through Hydrogen Transfer Reactions
resolves10.1002/cssc.201601121Catalytic Upstream Biorefining through Hydrogen Transfer Reactions: Understanding the Process from the Pulp Perspective
resolves10.1039/c7gc01324hIntegrating lignin valorization and bio-ethanol production: on the role of Ni-Al
<sub>2</sub>
O
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resolves10.1039/c7se00535kLignin-first biorefinery: a reusable catalyst for lignin depolymerization and application of lignin oil to jet fuel aromatics and polyurethane feedstock
resolves10.1002/cssc.201802130Task‐Specific Catalyst Development for Lignin‐First Biorefinery toward Hemicellulose Retention or Feedstock Extension
resolves10.1039/c8gc03440kMetal–acid nanoplate-supported ultrafine Ru nanoclusters for efficient catalytic fractionation of lignin into aromatic alcohols
resolves10.1039/c7fd00039aSelective production of mono-aromatics from lignocellulose over Pd/C catalyst: the influence of acid co-catalysts
resolves10.1021/acssuschemeng.9b01497Catalytic Conversion of Lignin in Woody Biomass into Phenolic Monomers in Methanol/Water Mixtures without External Hydrogen
resolves10.1002/cctc.201600235The Influence of Hemicellulose Sugars on Product Distribution of Early‐Stage Conversion of Lignin Oligomers Catalysed by Raney Nickel
resolves10.1039/c7fd00069cEffect of methanol in controlling defunctionalization of the propyl side chain of phenolics from catalytic upstream biorefining
resolves10.1039/c8gc03511cChemodivergent hydrogenolysis of eucalyptus lignin with Ni@ZIF-8 catalyst
resolves10.1002/cssc.201802847Fractionation of Lignocellulosic Biomass over Core–Shell Ni@Al<sub>2</sub>O<sub>3</sub> Catalysts with Formic Acid as a Cocatalyst and Hydrogen Source
resolves10.1002/cssc.201802497Lignin Valorization by Cobalt‐Catalyzed Fractionation of Lignocellulose to Yield Monophenolic Compounds
resolves10.1039/c7ra11947jLignin-first depolymerization of native corn stover with an unsupported MoS
<sub>2</sub>
catalyst
resolves10.1021/acscatal.8b03965Elucidating Interaction between Palladium and N-Doped Carbon Nanotubes: Effect of Electronic Property on Activity for Nitrobenzene Hydrogenation
resolves10.1039/c7ta01424dOne-pot synthesis of highly activated carbons from melamine and terephthalaldehyde as electrodes for high energy aqueous supercapacitors
resolves10.1107/s0909049505012719<i>ATHENA</i>,<i>ARTEMIS</i>,<i>HEPHAESTUS</i>: data analysis for X-ray absorption spectroscopy using<i>IFEFFIT</i>
resolves10.1016/j.apenergy.2016.03.093Non-catalytic upgrading of fast pyrolysis bio-oil in supercritical ethanol and combustion behavior of the upgraded oil
resolves10.1093/nsr/nwy048Single-atom heterogeneous catalysts based on distinct carbon nitride scaffolds
resolves10.1002/adma.201900509Pd Single‐Atom Catalysts on Nitrogen‐Doped Graphene for the Highly Selective Photothermal Hydrogenation of Acetylene to Ethylene
resolves10.1016/j.apcata.2017.04.022Selective hydrogenolysis of α O 4, β O 4, 4 O 5 C O bonds of lignin-model compounds and lignin-containing stillage derived from cellulosic bioethanol processing
resolves10.1039/c3nr05380fNitrogen-doped, carbon-rich, highly photoluminescent carbon dots from ammonium citrate
resolves10.1039/c4cc08735fNitrogen-doped carbon dots decorated on graphene: a novel all-carbon hybrid electrocatalyst for enhanced oxygen reduction reaction
resolves10.1038/srep23224Effects of Microporosity and Surface Chemistry on Separation Performances of N-Containing Pitch-Based Activated Carbons for CO2/N2 Binary Mixture
resolves10.1021/acscatal.7b02335Metal/Porous Carbon Composites for Heterogeneous Catalysis: Old Catalysts with Improved Performance Promoted by N-Doping
resolves10.1002/anie.201802231A Durable Nickel Single‐Atom Catalyst for Hydrogenation Reactions and Cellulose Valorization under Harsh Conditions
resolves10.1038/s41565-018-0167-2A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling
resolves10.1021/jp012769jA View from the Inside: Complexity in the Atomic Scale Ordering of Supported Metal Nanoparticles
resolves10.1002/anie.201902136Atom‐by‐Atom Resolution of Structure–Function Relations over Low‐Nuclearity Metal Catalysts
resolves10.1038/s41467-019-09986-1Differences in S/G ratio in natural poplar variants do not predict catalytic depolymerization monomer yields
resolves10.1039/c9gc00986hKinetic and mechanistic insights into hydrogenolysis of lignin to monomers in a continuous flow reactor
resolves10.1002/cssc.202000753Mechanistic Study of Diaryl Ether Bond Cleavage during Palladium‐Catalyzed Lignin Hydrogenolysis
resolves10.1039/c8gc00629fGa-doped Cu/H-nanozeolite-Y catalyst for selective hydrogenation and hydrodeoxygenation of lignin-derived chemicals
resolves10.1039/c8gc03623cHighly-efficient and magnetically-separable ZnO/Co@N-CNTs catalyst for hydrodeoxygenation of lignin and its derived species under mild conditions
resolves10.1039/c7gc00432jDirect conversion of cellulose to high-yield methyl lactate over Ga-doped Zn/H-nanozeolite Y catalysts in supercritical methanol
resolves10.1016/j.apcatb.2018.10.036One-pot di- and polysaccharides conversion to highly selective 2,5-dimethylfuran over Cu-Pd/Amino-functionalized Zr-based metal-organic framework (UiO-66(NH2))@SGO tandem catalyst
resolves10.1039/c7fd00036gNew catalytic strategies for α,ω-diols production from lignocellulosic biomass
resolves10.1126/science.aaf7810Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization
resolves10.1039/c7gc03417bLignin extraction and catalytic upgrading from genetically modified poplar
resolves10.1021/ja00100a006Pathway of p-Coumaric Acid Incorporation into Maize Lignin As Revealed by NMR
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