Search results for "sonogashira reaction"

showing 5 items of 5 documents

DEEP EUTECTIC SOLVENTS E LIQUIDI IONICI: SOLVENTI PER LO SVILUPPO DI PROCESSI ECO-COMPATIBILI

2020

L’obiettivo di questi tre anni di Dottorato è stato lo studio e l’utilizzo nuovi solventi di reazione in grado di sostituire i solventi organici classici. In particolare sono stati studiati i Deep Eutectic Solvent (DES) e le miscele di Liquidi Ionici (IL). I DES sono stati utilizzati come solventi per lo studio di reazioni organiche, usate per la formazione di nuovi legami C-C. Nello specifico sono state studiate la reazione di Diels-Alder, e diverse reazioni di coupling C-C catalizzate da Pd. In seguito, i DES sono stati utilizzati per la formazione di nuovi gel supramolecolari, chiamati eutectogel. Questi gel sono stati formati usando come gelator amminoacidi naturali, consentendo quindi …

Green Chemistry Deep Eutectic Solvents Solventi Liquidi Ionici Eutectogel gel supramolecolari Diels-Alder solventi alternativi Reazione di accoppiamento C-C Reazione di Suzuki 5-HMF Biomasse Disidratazione di carboidrati Fruttosio Glucosio Saccarosio Processi Eco-compatibili.Settore CHIM/06 - Chimica OrganicaGreen Chemistry Deep Eutectic Solvents Solvents Ionic Liquids Eutectogel supramolecular gels Diels-Alder alternative solvents Cross Coupling Reaction Suzuki Reaction Sonogashira Reaction Heck Reaction Hiyama Reaction 5-HMF Biomass carbohydrate dehydration Fructose Glucose Saccarose.
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Sustainable Approach to Waste-Minimized Sonogashira Cross-Coupling Reaction Based on Recoverable/Reusable Heterogeneous Catalytic/Base System and Ace…

2016

In this contribution, we present a chemically efficient and sustainable protocol for the palladium-catalyzed copper-free Sonogashira cross-coupling reaction, based on the use of a heterogeneous catalytic system. This consists in the combination of a palladium catalyst on highly cross-linked thiazolidine network on silica and a polystyrene-supported base. The solid catalyst/base system acts as a palladium scavenger avoiding leaching of the metal and consequent product contamination. The reaction can be conducted in safe and easily recoverable acetonitrile/water azeotrope as reaction medium. This proved to be an efficient greener alternative to the classic toxic aprotic media commonly used in…

Green chemistryAzeotrope media; Green chemistry; Heterogeneous catalysis; Sonogashira reaction; Waste minimization; Chemistry (all); Environmental Chemistry; Chemical Engineering (all); Renewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringWaste minimizationchemistry.chemical_elementSonogashira coupling010402 general chemistryHeterogeneous catalysis01 natural sciencesCoupling reactionCatalysisHeterogeneous catalysichemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryChemical Engineering (all)Renewable EnergyAcetonitrileHeterogeneous catalysisSustainability and the Environment010405 organic chemistryRenewable Energy Sustainability and the EnvironmentChemistry (all)Settore CHIM/06 - Chimica OrganicaGeneral ChemistryAzeotrope mediaCombinatorial chemistry0104 chemical scienceschemistryGreen chemistryLeaching (metallurgy)Sonogashira reactionPalladiumACS Sustainable Chemistry and Engineering
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Recyclable heterogeneous palladium catalysts in pure water: sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryheterogeneous palladium catalysts010405 organic chemistrywaterSonogashira couplingchemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energySuzuki reaction -Tsuji-Trost reaction0104 chemical sciencesCatalysisTsuji–Trost reaction[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactionchemistrySuzuki reactionHeck reactionOrganic chemistrySonogashira reactionComputingMilieux_MISCELLANEOUSPalladium
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Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations

2007

Conjugated alkynes are recurring building blocks in natural products, a wide range of industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for optics and electronics. The palladium-catalyzed cross-coupling between sp(2)-hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with sp-hybridized carbon atoms of terminal acetylenes is one of the most important developments in the field of alkyne chemistry over the past 50 years. The seminal work of the 1970s has initiated an intense search for more general and reliable reaction conditions. The interest in the catalytic activation of demanding substrates, the need to minimize the consumption of depletive r…

chemistry.chemical_elementSonogashira couplingAlkyneHalideConjugated systemHeterogeneous catalysis010402 general chemistryalkynes01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisOrganometallic Compoundscross-couplingOrganic chemistryComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationMolecular Structure010405 organic chemistryArylStereoisomerismGeneral ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/Catalysissonogashira reactionspalladiumCombinatorial chemistry0104 chemical sciencesheterogeneous catalysischemistryCarbonPalladium
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Functional molecular materials: supramolecular networks and coordination polymers with optical and/or magnetic properties

2020

El camp dels materials moleculars atrau l’atenció de molts científics degut al gran potencial de la química molecular en el disseny de materials amb un ajust precís de les seues propietats. Els dos projectes tractats en aquesta tesi representen dos temes que destaquen en aquesta àrea, materials de transició d’espín i polímers de coordinació amb propietats òptiques i/o magnètiques, gràcies al seu significant progrés i ràpid desenvolupament en els últims anys. La primera part d’aquesta tesi es basa en l’ús d’enllaços d’hidrogen en el disseny de xarxes multifuncionals de ferro(II) amb transicions d’espín abruptes. El capítol 1 és una introducció a aquest tema des de la perspectiva dels complex…

sonogashira reactionpicolinatespin crossoverUNESCO::QUÍMICAhydrogen bondsferroelectricsiron(II) complexesproton migrationisomerisationsensing experiments:QUÍMICA [UNESCO]
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