Search results for "Env"

showing 10 items of 30409 documents

Photochemically Produced Singlet Oxygen: Applications and Perspectives

2018

This Review aims to provide early stage researchers with an updated guide to applications of photochemically produced singlet oxygen and, at the same time, widen the experienced researcher's perspectives in a holistic approach to singlet oxygen chemistry. Without being exhaustive, literature between 2010 and early 2018 has been surveyed by focusing on a critical evaluation of new knowledge and applications. After an introductory section concerning singlet oxygen production, detection, and interactions with biological systems, subsequent sections describe current applications of singlet-oxygen-enabled technology. Besides strictly chemical synthesis applications, attention has been given to t…

010405 organic chemistryChemistryEnvironmental remediationSinglet oxygenmedicine.medical_treatmentOrganic ChemistryPhotodynamic therapySettore CHIM/06 - Chimica Organica010402 general chemistryPhotochemistry01 natural sciencessinglet oxygen0104 chemical sciencesAnalytical Chemistryphotooxygenation reactionchemistry.chemical_compoundphotodynamic therapymedicinePhysical and Theoretical Chemistryenvironmental remediationphototherapy
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Assembling Halogen-Bonded Capsules via Cation Exchange

2017

Dr. Lotta Turunen is currently a postdoctoral researcher within Acad. Prof. Kari Rissanen's research group at the University of Jyvaskyla in Finland. Under his supervision, she obtained her MSc in organic chemistry and completed her PhD in chemistry in late September 2017. Her research focused on designing, synthesizing, and characterizing halogen-bonded supramolecular assemblies, capsules, and cages.

010405 organic chemistryChemistryGeneral Chemical EngineeringBiochemistry (medical)Supramolecular chemistryNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesGroup (periodic table)HalogenMaterials ChemistryEnvironmental ChemistryOrganic chemistryChem
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Recent progress in the application of fluorinated chiral sulfinimine reagents

2018

Abstract The development of synthetic methodology allowing for a strategic incorporation of fluorine into target compounds is in a high demand in many areas of the chemical and pharmaceutical industries. In this regard, application of fluorinated chiral sulfinimine reagents, in particularly, N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine, is one of the most general and practical approaches for preparation of compounds containing pharmacophoric fluoro-amino-keto/hydroxy moieties. This article provides a timely and comprehensive overview of the recent synthetic applications of fluorinated chiral sulfinimine reagents for asymmetric synthesis of fluoro-containing polyfunctional amino-compound…

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisAsymmetric synthesisFluoro-imineAmino compounds010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesInorganic ChemistrySulfinimineReagentEnvironmental ChemistryPhysical and Theoretical ChemistryAmino compounds; Asymmetric synthesis; Fluoro-imine; Sulfinimine; Biochemistry; Environmental Chemistry; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic ChemistryJournal of Fluorine Chemistry
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The history and future challenges associated with the hydrogenation of vinyl fluorides

2018

Abstract Catalytic hydrogenation is one of the most powerful transformations available in synthetic chemistry; there have been three Nobel Laureates rewarded for their work in the field. Despite the advances in substrate scope and the development of enantioselective versions of this transformation, vinyl fluorides remain somewhat underrepresented. Successful hydrogenation of vinyl fluorides can give rise to a fluorine-containing stereocenter, an important feature which has great potential in many areas of chemistry. This review aims to explore the history of vinyl fluorides as substrates in hydrogenation reactions, and to highlight modern day challenges and unresolved issues regarding this …

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisNanotechnology010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesStereocenterInorganic ChemistryEnvironmental ChemistryPhysical and Theoretical ChemistryCatalytic hydrogenationJournal of Fluorine Chemistry
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Selective Formation of 4,4'-Biphenols by Anodic Dehydrogenative Cross- and Homo-Coupling Reaction.

2019

A simple and selective electrochemical synthesis by dehydrogenative coupling of unprotected 2,6- or 2,5-substituted phenols to the desired 4,4'-biphenols is reported. Using electricity as the oxidizing reagent avoids pre-functionalization of the starting materials, since a selective activation of the substrates takes place. Without the necessity for metal-catalysts or the use of stoichiometric reagents it is an economic and environmentally friendly transformation. The elaborated electrochemical protocol leads to a broad variety of the desired 4,4'-biphenols in a very simplified manner compared to classical approaches. This is particular the case for the cross-coupled products.

010405 organic chemistryChemistryOrganic ChemistryGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCatalysisCoupling reaction0104 chemical sciencesAnodeReagentOxidizing agentDehydrogenationStoichiometryChemistry (Weinheim an der Bergstrasse, Germany)
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Strecker reactions with hexacyanoferrates as non-toxic cyanide sources

2019

The Strecker reaction is the most widely applied three-component reaction. Although highly useful for the preparation of α-amino nitriles, α-amino acids, hydantoins and numerous related compounds, the need for the application of toxic sources of HCN limits its application in both academic and industrial settings. Here, we present a facile protocol for Strecker reactions using a mixture of potassium ferri- and ferrocyanides as a non-toxic substitute.

010405 organic chemistryCyanidePotassiumStrecker amino acid synthesischemistry.chemical_element010402 general chemistry01 natural sciencesPollution0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental ChemistryOrganic chemistryFerrocyanideGreen Chemistry
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Hierarchical Beta zeolites as catalysts in a one-pot three-component cascade Prins–Friedel–Crafts reaction

2020

Hierarchical Beta zeolites obtained from concentrated reaction mixtures (H2O/Si = 2.5–7.0) in the presence of CTAB and their conventional and nanosponge analogues were investigated in a one-pot cascade environmentally friendly Prins–Friedel–Crafts reaction of butyraldehyde with 3-buten-1-ol and anisole under mild conditions (60 °C). The highest yields of the desired products with 4-aryltetrahydropyran structure were achieved when using hierarchical zeolites characterised by well-developed mesoporosity (facilitating the formation of bulky intermediates and products) and by an increased fraction of highly accessible (evaluated by TTBPy method) medium-strength Bronsted acid sites. Acid sites w…

010405 organic chemistryEther010402 general chemistryAnisole01 natural sciencesPollutionEnvironmentally friendly0104 chemical sciencesCatalysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistryEnvironmental ChemistryOrganic chemistryButyraldehydeBrønsted–Lowry acid–base theoryFriedel–Crafts reactionComputingMilieux_MISCELLANEOUSGreen Chemistry
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2-Methyltetrahydrofuran: A Green Solvent for Iron-Catalyzed Cross-Coupling Reactions

2018

Iron‐catalyzed cross‐coupling reactions allow sustainable formation of C−C bonds using cost‐effective, earth‐abundant base‐metal catalysis for complex syntheses of pharmaceuticals, natural products, and fine chemicals. The major challenge to maintain full sustainability of the process is the identification of green and renewable solvents that can be harnessed to replace the conventional solvents for this highly attractive reaction. Herein, iron‐catalyzed cross‐coupling of aryl chlorides and tosylates with challenging organometallic reagents possessing β‐hydrogens is found to proceed in good to excellent yields with the green, sustainable, and eco‐friendly 2‐methyltetrahydrofuran (2‐MeTHF) a…

010405 organic chemistryGeneral Chemical EngineeringAryl2-MethyltetrahydrofuranHomogeneous catalysis010402 general chemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesCatalysisSolventchemistry.chemical_compoundGeneral EnergychemistryReagentFunctional groupEnvironmental ChemistryGeneral Materials ScienceChemSusChem
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A metal-free and regioselective approach to (Z)-β-fluorovinyl sulfones and their chemoselective hydrogenation to β-fluoroalkyl sulfones

2018

Abstract A highly regioselective, metal-free hydrofluorination reaction of alkynyl sulfones was developed using TBAF—one of the cheapest and most commonly available fluoride sources. In addition, the reactivity of the resulting β-fluorovinyl sulfones was studied, focusing on their selective hydrogenation reaction. Both β-fluorovinyl sulfones and their hydrogenation products β-fluoroalkyl sulfones may find applications in medicinal and agrochemical sciences.

010405 organic chemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryHydrogenation reactionEnvironmental ChemistryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryFluorideJournal of Fluorine Chemistry
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A thermally/chemically robust and easily regenerable anilato-based ultramicroporous 3D MOF for CO 2 uptake and separation

2021

The combination of the properly designed novel organic linker, 3,6-N-ditriazoyil-2,5-dihydroxy-1,4-benzoquinone (trz2An), with CoII ions results in a 3D ultramicroporous MOF with high CO2 uptake capacity and separation efficiency, with particular attention to CO2/N2 and CO2/CH4 gas mixtures. This material consists of 1D chains of octahedrally coordinated CoII ions linked through the anilato ligands in the equatorial positions and to the triazole substituents from two neighbouring chains in the two axial positions. This leads to a 3D microporous structure with voids with an affinity for CO2 molecules and channels that enable the selective entrance of CO2 but not of molecules with larger kine…

010405 organic chemistryRenewable Energy Sustainability and the EnvironmentUNESCO::QUÍMICAHigh selectivityTriazoleGeneral ChemistryMicroporous materialQuímica010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]0104 chemical sciencesIonchemistry.chemical_compoundAdsorptionchemistryChemical engineeringCarbon dioxideMoleculeGeneral Materials ScienceLinkerMaterialsKinetic diameterJournal of Materials Chemistry A
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