Search results for "GREEN"

showing 10 items of 1660 documents

Examples of xylochemistry: colorants and polymers

2017

Against the backdrop of modern sustainable chemistry and valorization of biomass for chemical raw materials, the syntheses of indigo dyes and polyamides as representatives of two classes of everyday chemical products based on xylochemicals are described. Wood-derived starting materials were transformed into functional materials using the principles of green chemistry to expand the scope of products gained from renewable resources. The indigo dyes were synthesized in a short, straightforward sequence starting from vanillin. Two polyamides, representatives of an important class of polymers, were obtained from 4-propylcyclohexanol, which is one of the longest known (and most abundant) hydrogen…

Green chemistrychemistry.chemical_classification010405 organic chemistryDepolymerizationVanillinPolymerRaw material010402 general chemistry01 natural sciencesPollutionIndigo0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental ChemistryOrganic chemistryLigninRenewable resourceGreen Chemistry
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Sustainable access to biobased biphenol epoxy resins by electrochemical dehydrogenative dimerization of eugenol

2019

Limited fossil resources require innovative monomers and polymers derived from renewable feedstocks such as plant biomass. Thermosetting epoxy resins largely rely on petrochemical bisphenol-type monomers, which give high performance materials but are controversial due to their effects on human health. Herein, we present two biobased epoxy resins by direct dehydrogenative dimerization of eugenol, the main component of clove oil. Taking the Principles of Green Chemistry into account, we developed electrochemical dehydrodimerization at reticulated vitreous carbon (RVC) electrodes using methanol as environmentally benign solvent. Thus, fluorinated solvents such as 1,1,1,3,3,3-hexafluoroisopropa…

Green chemistrychemistry.chemical_classification010405 organic chemistryThermosetting polymerPolymerEpoxy010402 general chemistry01 natural sciencesPollution0104 chemical sciencesSolventchemistry.chemical_compoundPetrochemicalchemistryvisual_artvisual_art.visual_art_mediumEnvironmental ChemistryOrganic chemistryMethanolCuring (chemistry)Green Chemistry
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Cyclic dipeptides: catalyst/promoter-free, rapid and environmentally benign cyclization of free amino acids

2011

“The best catalyst is no catalyst.” With growing public concern over global warming and the amount of greenhouse gases, it is important to reduce the amount of chemicals and eliminate waste, to obtain better results in a simple, selective, safe, and environmentally benign fashion compared to conventional tedious chemical synthesis. Herein, we disclose an environmentally benign, rapid, catalyst/promoter/coupling reagent-free cyclization procedure of free amino acids to furnish exclusively cyclic dipeptides (2,5-diketopiperazines, DKPs) in excellent or even quantitative yield, along with their solid state self-assembling properties. This process is extremely simple and highly efficient with l…

Green chemistrychemistry.chemical_classificationCyclic compoundChemistryPollutionChemical synthesisCyclic peptideCatalysisSolventYield (chemistry)Environmental ChemistryOrganic chemistrySelectivityta116Green Chemistry
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Uncommon perspectives in palladium- and copper-catalysed arylation and heteroarylation of terminal alkynes following Heck or Sonogashira protocols: I…

2013

Abstract Conjugated alkynes are recurring building blocks in natural products and in a wide range of important compounds, such as pharmaceuticals, agrochemicals, or molecular materials. The palladium-catalysed cross-coupling reaction between the sp 2 -hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with the sp -hybridized carbon atoms of terminal alkynes is one of the most important developments in the field of alkyne chemistry over the past 50 years. Room for improvement still exists in these important reactions of direct arylation of terminal alkynes. In this prospect, the present authors have developed several strategies aiming at improving the reactivity, the selectivity,…

Green chemistrychemistry.chemical_classificationGeneral Chemical EngineeringArylchemistry.chemical_elementAlkyneSonogashira couplingGeneral ChemistryCombinatorial chemistrychemistry.chemical_compoundchemistryIonic liquidOrganic synthesisReactivity (chemistry)PalladiumComptes Rendus Chimie
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Sustainable and cost-efficient electro-synthesis of formamidine acetate from cyanamide in aqueous acidic electrolyte

2021

Formamidine represents a versatile building block in synthetic organic chemistry. We developed a new electrochemical synthesis of formamidine acetate by cathodic reduction of cyanamide in an aqueous electrolyte and in high yield. The crude product could be used for further conversions, such as to pyrimidines without purification. Compared to established synthetic routes neither prior processing of cyanamide was necessary, nor precious transition-metal catalyst were required, nor any reagent waste was produced, and only biocompatible and sustainable solvents were employed for this process, following the requirements of green chemistry.

Green chemistrychemistry.chemical_compoundAqueous solutionchemistryReagentYield (chemistry)Environmental ChemistryOrganic chemistryCyanamideElectrolyteElectrochemistryPollutionCatalysisGreen Chemistry
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Photocatalytic Partial Oxidation of 5‐Hydroxymethylfurfural (HMF) to 2,5‐Diformylfuran (DFF) Over a Covalent Triazine Framework in Water

2020

Green chemistrychemistry.chemical_compoundChemistryCovalent bond5-hydroxymethylfurfuralOrganic ChemistryPhotocatalysisOrganic chemistryPartial oxidationPhysical and Theoretical ChemistryHydroxymethylfurfuralAnalytical ChemistryTriazineChemPhotoChem
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Dehydrogenative Anodic Cyanation Reaction of Phenols in Benzylic Positions

2019

Green chemistrychemistry.chemical_compoundChemistryElectrochemistryOrganic chemistryPhenolsCyanationElectrochemistryCatalysisAnodeChemElectroChem
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Evaluation of Antiradical Activity and Reducing Capacity of Synthesised Bispyridinium Dibromides Obtained by Quaternisation of 4-Pyridyl-1,4-dihydrop…

2015

New bispyridinium dibromides based on the 1,4-dihydropyridine (1,4-DHP) cycle were synthesised in the reaction between 4-pyridyl-1,4-DHP derivatives and propargyl bromide. It has been shown that variation of the substituent position on the pyridine as well as small changes in the electronic nature of the 1,4-DHP cycle as a result of the substituent nature at the 3 and 5 positions do not affect the course of the reaction and in all cases the corresponding bispyridinium dibromides 4a–e were formed. The antiradical activity, using 1,1-diphenyl-2-picrylhydrazine as a free radical scavenger, and the reducing capacity using phosphomolybdenum complexes have been evaluated for the newly synthesise…

Green chemistrychemistry.chemical_compoundReaction mechanismchemistryBiocatalysisPyridineSubstituentSupramolecular chemistryOrganic chemistryGeneral ChemistryPropargyl bromideFree radical scavengerMedicinal chemistryAustralian Journal of Chemistry
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Frontispiece: A Novel Cathode Material for Cathodic Dehalogenation of 1,1‐Dibromo Cyclopropane Derivatives

2015

Green chemistrychemistry.chemical_compoundchemistryCathode materialOrganic ChemistryInorganic chemistryOrganic chemistryHalogenationGeneral ChemistryCatalysisCyclopropaneCathodic protectionChemistry – A European Journal
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Metal‐Free Twofold Electrochemical C−H Amination of Activated Arenes: Application to Medicinally Relevant Precursor Synthesis

2020

Abstract The efficient production of many medicinally or synthetically important starting materials suffers from wasteful or toxic precursors for the synthesis. In particular, the aromatic non‐protected primary amine function represents a versatile synthetic precursor, but its synthesis typically requires toxic oxidizing agents and transition metal catalysts. The twofold electrochemical amination of activated benzene derivatives via Zincke intermediates provides an alternative sustainable strategy for the formation of new C−N bonds of high synthetic value. As a proof of concept, we use our approach to generate a benzoxazinone scaffold that gained attention as a starting structure against ca…

Green chemistrydrug scaffoldPrimary (chemistry)Full Paper010405 organic chemistryChemistrybenzoxazinoneOrganic ChemistryGeneral ChemistryFull Papers010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysiselectrochemistrytwofold aminationMetal freeOxidizing agentsustainable chemistryAmine gas treatingSynthetic MethodsAminationChemistry – A European Journal
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