Search results for "allied"

showing 10 items of 108 documents

Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

2020

Abstract A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N‐protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

Green chemistry540 Chemistry and allied sciencesDeblocking filterSupporting electrolyteRadicalSustainable Chemistry010402 general chemistryElectrochemistry01 natural sciencesCatalysisCoupling reactionNC couplingProtecting groupgreen chemistry010405 organic chemistryChemistryCommunicationOrganic Chemistryheterocyclic chemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical sciencesAnodecarbazoleselectrochemistry540 Chemie
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Selective and Scalable Electrosynthesis of 2H-2-(Aryl)-benzo[d]-1,2,3-triazoles and Their N-Oxides by Using Leaded Bronze Cathodes.

2020

Abstract Electrosynthesis of 2H‐2‐(aryl)benzo[d]‐1,2,3‐triazoles and their N‐oxides from 2‐nitroazobenzene derivatives is reported. The electrolysis is conducted in a very simple undivided cell under constant current conditions with a leaded bronze cathode and a glassy carbon anode. The product distribution between 2H‐2‐(aryl)benzo[d]‐1,2,3‐triazoles and their N‐oxides can be guided by simply controlling the current density and the amount of the charge applied. The reaction tolerates several sensitive functional groups in reductive electrochemistry. The usefulness and the applicability of the synthetic method is demonstrated by a formal synthesis of an antiviral compound.

Green chemistry540 Chemistry and allied sciencesazo compoundsreductionGlassy carbon010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawsustainable chemistryElectrolysis010405 organic chemistryChemistryArylCommunicationOrganic ChemistryGeneral ChemistryCombinatorial chemistryCathodeCommunications0104 chemical sciencesAnodeElectrochemistry | Hot Paperelectrochemistry540 Chemienitrogen heterocyclesChemistry (Weinheim an der Bergstrasse, Germany)
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Straightforward Electrochemical Sulfonylation of Arenes and Aniline Derivatives using Sodium Sulfinates

2019

Green chemistry540 Chemistry and allied scienceschemistry.chemical_compoundAnilineChemistry540 ChemieSodiumElectrochemistrychemistry.chemical_elementOrganic chemistryElectrochemistryCatalysisChemElectroChem
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Developments in the dehydrogenative electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol

2021

Abstract The symmetric biphenol 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol is a well‐known ligand building block and is used in transition‐metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro‐organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the …

Green chemistry540 Chemistry and allied sciencespolycycles010405 organic chemistryChemistryoxidationOrganic ChemistryC−C couplingMinireviewsGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesC c couplingelectrochemistry540 Chemiesustainable chemistryMinireviewC−C Coupling | Reviews Showcase
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Electrochemical nitration with nitrite

2021

Aromatic nitration has tremendous importance in organic chemistry as nitroaromatic compounds serve as versatile building blocks. This study represents the electrochemical aromatic nitration with NBu4 NO2 , which serves a dual role as supporting electrolyte and as a safe, readily available, and easy-to-handle nitro source. Stoichiometric amounts of 1,1,1-3,3,3-hexafluoroisopropan-2-ol (HFIP) in MeCN significantly increase the yield by solvent control. The reaction mechanism is based on electrochemical oxidation of nitrite to NO2 , which initiates the nitration reaction in a divided electrolysis cell with inexpensive graphite electrodes. Overall, the reaction is demonstrated for 20 examples w…

Green chemistryReaction mechanism540 Chemistry and allied sciencesSupporting electrolyteGeneral Chemical EngineeringElectrochemistryCombinatorial chemistrySolventchemistry.chemical_compoundGeneral EnergychemistryNitrationYield (chemistry)540 ChemieEnvironmental ChemistryGeneral Materials ScienceNitrite
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NanoSr - A New Carbonate Microanalytical Reference Material for In Situ Strontium Isotope Analysis

2019

The in situ measurement of Sr isotopes in carbonates by MC‐ICP‐MS is limited by the availability of suitable microanalytical reference materials (RMs), which match the samples of interest. Whereas several well‐characterised carbonate reference materials for Sr mass fractions > 1000 µg g−1 are available, there is a lack of well‐characterised carbonate microanalytical RMs with lower Sr mass fractions. Here, we present a new synthetic carbonate nanopowder RM with a Sr mass fraction of ca. 500 µg g−1 suitable for microanalytical Sr isotope research (‘NanoSr’). NanoSr was analysed by both solution‐based and in situ techniques. Element mass fractions were determined using EPMA (Ca mass fraction),…

In situ540 Chemistry and allied sciences551.9Laser ablationMaterials scienceMc icp msStrontium isotopes; Laser ablation; Reference material; Calcium carbonate; Nanopowder; MC‐ICP‐MSRadiochemistryNanopowderGeologyStrontium isotopesLaser ablationIsotopes of strontium550 Geowissenschaftenchemistry.chemical_compoundCalcium carbonateMC‐ICP‐MSchemistry550 Earth sciencesGeochemistry and Petrology540 ChemieCarbonateReference materialMC-ICP-MSCalcium carbonate
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Constitution and conductivity of metalloporphyrin tapes

2020

Inorganic Chemistry540 Chemistry and allied sciencesChemical engineeringChemistryConstitutionmedia_common.quotation_subject540 ChemieOxidative coupling of methaneChemical vapor depositionConductivityThin filmmedia_common
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Unexpected C–C bond formation with a ferrocenyl Fischer carbene complex

2020

Inorganic ChemistryC c couplingchemistry.chemical_compoundChromium540 Chemistry and allied sciencesFerrocenechemistryTransition metal carbene complex540 Chemiechemistry.chemical_elementBond formationMedicinal chemistry
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The Use of the Macrocyclic Chelator DOTA in Radiochemical Separations

2019

Inorganic ChemistryChemical separation540 Chemistry and allied scienceschemistry.chemical_compoundchemistry540 ChemieKineticsRadiochemistryDOTAChelationEuropean Journal of Inorganic Chemistry
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Bridging rigidity and flexibility : modulation of supramolecular hydrogels by metal complexation

2021

The combination of complementary, noncovalent interactions is a key principle for the design of multistimuli responsive hydrogels. In this work, an amphiphilic peptide, supramacromolecular hydrogelator which combines metal-ligand coordination induced gelation and thermoresponsive toughening is reported. Following a modular approach, the incorporation of the triphenylalanine sequence FFF into a structural (C3EG ) and a terpyridine-functionalized (C3Tpy ) C3 -symmetric monomer enables their statistical copolymerization into self-assembled, 1D nanorods in water, as investigated by circular dichroism (CD) spectroscopy and transmission electron microscopy (TEM). In the presence of a terpyridine …

Ionschemistry.chemical_classificationCircular dichroism540 Chemistry and allied sciencesPolymers and PlasticsOrganic ChemistryHydrogelsPolyethylene glycolPolyethylene Glycolschemistry.chemical_compoundMonomerchemistryChemical engineeringMetals540 ChemieAmphiphileSelf-healing hydrogelsMaterials ChemistryCopolymerNon-covalent interactionsTerpyridinePeptides
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