Search results for "Catalysis"

showing 10 items of 5944 documents

Xylochemistry--Making Natural Products Entirely from Wood.

2015

The first total synthesis of the dimeric berberine alkaloid ilicifoline (ilicifoline B) is reported. Its carbon skeleton is constructed from ferulic acid, veratrole, and methanol. The synthesis reported herein employs starting materials solely derived from wood. The natural product is thus constructed entirely from renewable resources. The same strategy is applied to a formal total synthesis of morphinan alkaloids. The use of wood-derived building blocks (xylochemicals) instead of the conventional petrochemicals represents a sustainable alternative to classical synthetic approaches.

Green chemistryBiological ProductsNatural productMolecular StructureBerberine AlkaloidsTotal synthesisGeneral ChemistryWoodCatalysisFerulic acidchemistry.chemical_compoundPetrochemicalchemistryOrganic chemistryMethanolBerberine AlkaloidsRenewable resourceAngewandte Chemie (International ed. in English)
researchProduct

Boosting the methanolysis of polycarbonate by the synergy between ultrasound irradiation and task specific ionic liquids

2021

In an attempt to perform polycarbonate chemical recycling in a more sustainable way, we took into consideration the combined use of ultrasound irradiation and task specific ionic liquids. Towards this aim, the methanolysis of polycarbonate, into dimethylcarbonate and bisphenol A, was carried out in the presence of cholinium-based ionic liquids featuring anions derived from amino acids and other eco-friendly species. The target process was optimized in terms of both energy and material amounts as well as in terms of the nature of the catalysts used. The proposed protocol allowed high conversion and yields of bisphenol A to be obtained, under milder conditions compared to the ones so far repo…

Green chemistryBisphenol AMaterials sciencegreen chemistryCombined usecatalysiSettore CHIM/06 - Chimica OrganicaPollutionCatalysischemistry.chemical_compoundChemical engineeringchemistryvisual_artScientific methodIonic liquidvisual_art.visual_art_mediumEnvironmental ChemistryPolycarbonateUltrasound irradiationDepolymerizationionic liquid
researchProduct

Activity of a Heterogeneous Catalyst in Deep Eutectic Solvents: The Case of Carbohydrate Conversion into 5-Hydroxymethylfurfural

2019

Obtaining industrially relevant products from renewable resources and developing processes under the light of sustainable chemistry is a prominent endeavor of present-day chemical research. In this context, herein we investigated the dehydration of fructose and sucrose in deep eutectic solvents promoted by the ion-exchange resin Amberlyst 15 as heterogeneous catalyst. We optimized the reaction conditions in terms of temperature, catalyst loading, and initial amount of substrate. Then, we looked at the effect of structural variations in the solvent components on the reaction outcome. Under the best experimental conditions, we obtained very good yields of 78% at 60 °C and 69% at 80 °C for fru…

Green chemistryChemical researchRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical EngineeringSettore CHIM/06 - Chimica Organica02 engineering and technologyGeneral ChemistryCarbohydrate010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciences0104 chemical sciencesChemical engineering5-hydroxymethylfurfuralEnvironmental ChemistryDeep eutectic solvents Amberyst 15 Carbohydrates 5-HMF Catalyst recycling0210 nano-technologyEutectic systemRenewable resourceACS Sustainable Chemistry & Engineering
researchProduct

Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-ol

2018

A selective dehydrogenative electrochemical functionalization of benzylic positions that employs 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP) has been developed. The electrogenerated products are versatile intermediates for subsequent functionalizations as they act as masked benzylic cations that can be easily activated. Herein, we report a sustainable, scalable, and reagent- and metal-free dehydrogenative formal benzyl-aryl cross-coupling. Liberation of the benzylic cation was accomplished through the use of acid. Valuable diarylmethanes are accessible in the presence of aromatic nucleophiles. The direct application of electricity enables a safe and environmentally benign chemical transformati…

Green chemistryChemical transformation010405 organic chemistryChemistryArylGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundNucleophileReagentvisual_artvisual_art.visual_art_mediumSurface modificationAngewandte Chemie International Edition
researchProduct

Inside Back Cover: Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-o…

2018

Green chemistryChemistryArylGeneral ChemistryElectrochemistryMedicinal chemistryCatalysisAnodeCoupling (electronics)Metalchemistry.chemical_compoundvisual_artReagentvisual_art.visual_art_mediumAngewandte Chemie International Edition
researchProduct

Front Cover: Selective and Scalable Electrosynthesis of 2H ‐2‐(Aryl)‐benzo[ d ]‐1,2,3‐triazoles and Their N‐Oxides by Using Leaded Bronze Cathodes (C…

2020

Green chemistryChemistryArylOrganic ChemistryInorganic chemistryGeneral Chemistryengineering.materialElectrochemistryElectrosynthesisCatalysisCathodelaw.inventionchemistry.chemical_compoundFront coverlawengineeringBronzeChemistry – A European Journal
researchProduct

Versatile Electrochemical C-H Amination via Zincke Intermediates.

2015

Simply by applying electricity, the amination reaction of a broad variety of arenes, heteroarenes, and benzylic substrates is achieved. Pyridine serves as the nitrogen source and the intermediate cationic species are well-protected from over-oxidation.

Green chemistryChemistryCationic polymerizationGeneral ChemistryElectrochemical TechniquesElectrochemistryCarbonCatalysischemistry.chemical_compoundPyridineOrganic chemistryOxidative coupling of methaneNitrogen sourceOxidation-ReductionAminationCopperAminationHydrogenAngewandte Chemie (International ed. in English)
researchProduct

Synthesis of 2,3‐Dihydro‐4‐pyridones, 4‐Quinolones, and 2,3‐Dihydro‐4‐azocinones by Visible‐Light Photocatalytic Aerobic Dehydrogenation

2019

Green chemistryChemistryOrganic Chemistry4-quinolonesPhotocatalysisDehydrogenationPhysical and Theoretical ChemistryVisible light photocatalyticPhotochemistryEuropean Journal of Organic Chemistry
researchProduct

A Novel Cathode Material for Cathodic Dehalogenation of 1,1-Dibromo Cyclopropane Derivatives.

2015

Leaded bronze turned out to be an excellent cathode material for the dehalogenation reaction of cyclopropanes without affecting the strained molecular entity. With this particular alloy, beneficial properties of lead cathodes are conserved, whereas the corrosion of cathode is efficiently suppressed. The solvent in the electrolyte determines whether a complete debromination reaction is achieved or if the process can be selectively stopped at the monobromo cyclopropane intermediate. The electroorganic conversion tolerates a variety of functional groups and can be conducted at rather complex substrates like cyclosporine A. This approach allows the sustainable preparation of cyclopropane deriva…

Green chemistryChemistryOrganic ChemistryAlloyInorganic chemistryHalogenationGeneral ChemistryElectrolyteengineering.materialCombinatorial chemistryCatalysisCathodeCyclopropanelaw.inventionCorrosionSolventchemistry.chemical_compoundlawengineeringChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Ionic liquids as precatalysts in the highly stereoselective conjugate addition of α,β-unsaturated aldehydes to chalcones.

2014

Imidazolium-based ionic liquids (ILs) serve both as recyclable reaction media and as precatalysts for the N-heterocyclic carbene-catalyzed conjugate addition of α,β-unsaturated aldehydes to chalcones. The reaction produces a broad scope of 1,6-ketoesters incorporating an anti-diphenyl moiety in high yields and with high stereoselectivity. In recycling experiments, the IL can be reused up to five times with retained reactivity and selectivity. Moreover, the 1,6-ketoesters form self-assembled organogels in aliphatic hydrocarbons. The reaction protocol is robust, easily operated, scalable and highly functionalized compounds can be obtained from inexpensive and readily accessible starting mater…

Green chemistryChemistryOrganic ChemistryGeneral ChemistryCatalysischemistry.chemical_compoundIonic liquidMoietyOrganic chemistryReactivity (chemistry)StereoselectivitySelectivityta116ConjugateChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct