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Flow "Fine" Synthesis: High Yielding and Selective Organic Synthesis by Flow MethodsTranscript and metabolite profiling for the evaluation of tobacco tree and poplar as feedstock for the bio-based industryComparative transcriptome analysis reveals different strategies for degradation of steam-exploded sugarcane bagasse by Aspergillus niger and Trichoderma reesei.Chitosan derivatives as important biorefinery intermediates. Quaternary tetraalkylammonium chitosan derivatives utilized in anion exchange chromatography for perchlorate removal.Harmonising production, properties and environmental consequences of liquid transport fuels from biomass--2,5-dimethylfuran as a case study.Transition-metal catalyzed valorization of lignin: the key to a sustainable carbon-neutral future.Co-production of 11α-hydroxyprogesterone and ethanol using recombinant yeast expressing fungal steroid hydroxylasesNovel pathways to 2,5-dimethylfuran via biomass-derived 5-(chloromethyl)furfural.Production of isoprene, one of the high-density fuel precursors, from peanut hull using the high-efficient lignin-removal pretreatment method.Upgrading Lignocellulosic Products to Drop-In Biofuels via Dehydrogenative Cross-Coupling and Hydrodeoxygenation Sequence.Lignocellulose-Biorefinery: Ethanol-Focused.The pangenome of the genus Clostridium.Microwave-Assisted γ-Valerolactone Production for Biomass Lignin Extraction: A Cascade Protocol.Penicillium janthinellum: a source of efficient and high levels of β-glucosidase.Deep Eutectic Solvents as Efficient Media for the Extraction and Recovery of Cynaropicrin from Cynara cardunculus L. Leaves.Biotechnological production of value-added compounds by ustilaginomycetous yeasts.Re-direction of carbon flux to key precursor malonyl-CoA via artificial small RNAs in photosynthetic Synechocystis sp. PCC 6803.Design of Organic Transformations at Ambient Conditions: Our Sincere Efforts to the Cause of Green Chemistry Practice.Metal organic frameworks as catalysts in solvent-free or ionic liquid assisted conditionsDesign for carbon–carbon bond forming reactions under ambient conditionsContinuous flow nanocatalysis: reaction pathways in the conversion of levulinic acid to valuable chemicals
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մարտին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Green chemistry, biofuels, and biorefinery.
@ast
Green chemistry, biofuels, and biorefinery.
@en
Green chemistry, biofuels, and biorefinery.
@nl
type
label
Green chemistry, biofuels, and biorefinery.
@ast
Green chemistry, biofuels, and biorefinery.
@en
Green chemistry, biofuels, and biorefinery.
@nl
prefLabel
Green chemistry, biofuels, and biorefinery.
@ast
Green chemistry, biofuels, and biorefinery.
@en
Green chemistry, biofuels, and biorefinery.
@nl
P1476
Green chemistry, biofuels, and biorefinery.
@en
P2093
Avtar S Matharu
James H Clark
P304
P356
10.1146/ANNUREV-CHEMBIOENG-062011-081014
P50
P577
2012-03-29T00:00:00Z