Search results for "Halogenation"

showing 10 items of 111 documents

Metal-Free and User-Friendly Regioselective Hydroxyfluorination of Olefins

2018

A simple, user-friendly, metal-free protocol for the regioselective anti-Markovnikov hydrofluorination of olefins using readily available and inexpensive reagents has been developed. This new approach displays a broader scope than previously reported methodologies and has been applied to the late-stage fluorination of a complex molecule, giving rise to a fluorosteroid derivative. The stereochemistry of the process has also been studied in some detail.

User FriendlyHalogenationMolecular Structure010405 organic chemistryOrganic ChemistryRegioselectivityAlkenes010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistryArticle0104 chemical scienceschemistry.chemical_compoundchemistryMetal freeMetalsPhysical and Theoretical ChemistryDerivative (chemistry)
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Breakthrough in the α-Perchlorination of Acyl Chlorides

2012

The preparation of -perchloroacyl chlorides, from reaction of the corresponding unfunctionalized acyl halides with chlorine, was efficiently achieved under base-catalysis, using a tetraalkylammonium chloride as catalyst. The process is solvent-free and the procedure is easy, inexpensive, and suitable for scale-up.

acid chlorideacyl chlorides halogenation chlorine base catalysisOrganic Chemistry2Halogenationchemistry.chemical_elementtetralkylammonium chlorideSettore CHIM/06 - Chimica Organicaacyl chloridesacid chloride perchlorination tetralkylammonium chlorideCatalysisAcylationacyl chlorides halogenation chlorine base catalysis 2; 2-dichloroacyl chlorideschemistry2-dichloroacyl chlorideshalogenationchlorineChlorineOrganic chemistryperchlorinationbase catalysis
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Poly-iodinated closo 1,2-C 2 B 10 and nido [7,8-C 2 B 9 ] − carborane frameworks: Synthesis and consequences

2015

Abstract The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their chemical shift position in the 1H NMR, and the lesser tendency to η5-coordination in parallel to a larger number of iodo groups.

carboranesSolvent freeStereochemistryChemistryOrganic ChemistryHalogenationsolvent freeBiochemistryInorganic ChemistryiodinationMaterials ChemistryProton NMRCarboranePhysical and Theoretical Chemistryta116acidityJournal of Organometallic Chemistry
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High-Performance Electron-Transporting Polymers Derived from a Heteroaryl Bis(trifluoroborate)

2011

In this communication, we report that dipotassium aryl bis(trifluoroborate)s make stable and easy-to-purify yet reactive monomers under Suzuki polycondensation reactions. A bis(trifluoroborate) of 2-alkylbenzotriazole was prepared successfully and copolymerized with dibromobenzothiadiazole in the presence of a Pd catalyst and LiOH, yielding high molecular weight conjugated polymers. This polymer (P1) composed of all electron-accepting units shows excellent electron-transport properties (μ(e) = 0.02 cm(2) V(-1) s(-1)), which proves the value of the aryl bis(trifluoroborate) monomers and suggests that many other types of semiconducting polymers that could not be accessed previously can be syn…

chemistry.chemical_classificationCondensation polymerHalogenationTransistors ElectronicPolymersArylRespiratory electron transportGeneral ChemistryPolymerTriazolesConjugated systemBiochemistryCatalysisCatalysisElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryBoratesPolymer chemistryJournal of the American Chemical Society
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Synthesis of brominated tetrathiafulvalenes via phosphite-mediated cross-coupling

2010

The synthesis of polybrominated tetrathiafulvalenes (TTF-Brn, 2-4) containing 2-4 bromine atoms via phosphite-mediated cross-coupling of bromo-substituted 1,3-dithiole-2-thiones and 1,3-dithiole-2-ones is reported. © 2010 Elsevier B.V.

chemistry.chemical_classificationKetoneBromineHalogenationLithiationChemistryMechanical EngineeringMetals and AlloysCross reactionschemistry.chemical_elementHalogenationCondensed Matter PhysicsChemical synthesisElectronic Optical and Magnetic MaterialsCoupling (electronics)Brominated tetrathiafulvalenesPhosphite cross-couplingMechanics of MaterialsPolymer chemistryMaterials ChemistryOrganic chemistrySynthetic Metals
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Oxidative halogenation of substituted pyrroles with Cu(II). PartIII. Bromination and chlorination of 2-benzoylpyrrole

1992

The bromination of 2-benzoylpyrrole with copper(II) bromide in the homogeneous and the heterogeneous phase is described, giving 4- and 5-monobromo derivatives whose ratio decreases as the temperature is increased. The same reaction with copper(II) chloride in acetonitrile at 60° produces 5-chloro-2-benzoylpyrrole as the major product. 4,5-Dihalopyrroles in good yields are obtained with an excess of halogenating agent.

chemistry.chemical_classificationKetoneChemistryOrganic ChemistryHalogenationchemistry.chemical_elementOxidative phosphorylationMedicinal chemistryChlorideCopperchemistry.chemical_compoundBromidePhase (matter)medicineOrganic chemistryAcetonitrilemedicine.drugJournal of Heterocyclic Chemistry
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Influence of the nature of the substrate and of operative parameters in the electrocarboxylation of halogenated acetophenones and benzophenones

2005

Abstract The electrocarboxylation of halogenated acetophenones and benzophenones to the corresponding hydroxycarboxylic acids has been carried out in undivided cell equipped with aluminium sacrificial anode and using 1-methyl-2-pyrrolidinone (NMP) as the solvent. The radical anion generated by the electro-reduction of the aromatic ketone is involved in several competitive reactions which lead to the formation of the target hydroxycarboxylic acid, the corresponding alcohol and pinacol and the de-halogenated parent ketone. If sufficiently negative working potentials are imposed, the latter is reduced to the corresponding carboxylate, pinacol and alcohol. Very different results in terms of sel…

chemistry.chemical_classificationKetonePinacolGeneral Chemical EngineeringCarboxylic acidHalogenationReductive dehalogenationAlcoholSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrocarboxylationchemistry.chemical_compoundchemistryCarboxylationRadical anionsHalobenzophenoneElectrochemistryOrganic chemistryHaloacetophenoneCarboxylateSelectivity
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4-Alkenyl-1,2,3-thiadiazole

1986

Die Titelverbindungen 5 werden aus entsprechenden Alkylderivaten durch Bromierung/Dehydrobromierung (Weg A) oder durch Wittig-Reaktion (Weg B) dargestellt. Mit 4-Phenyl-4H-1,2,4-triazol-3,5-dion entstehen unter Erhaltung des Thiadiazolrings die Monoaddukte 12. 4-Alkenyl-1,2,3-thiadiazoles The title compounds 5 are prepared from the corresponding alkyl derivatives by bromination/dehydrobromination (route A) or by Wittig reaction (route B). 4-Phenyl-4H-1,2,4-triazole-3,5-dione yields the monoadducts 12 by maintenance of the thiadiazole ring.

chemistry.chemical_classificationKetonechemistryOrganic ChemistryWittig reactionOrganic chemistryHalogenationNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryMedicinal chemistryAldehydeCycloadditionLiebigs Annalen der Chemie
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Functional Enzyme Mimics for Oxidative Halogenation Reactions that Combat Biofilm Formation

2017

Transition-metal oxide nanoparticles and molecular coordination compounds are highlighted as functional mimics of halogenating enzymes. These enzymes are involved in halometabolite biosynthesis. Their activity is based upon the formation of hypohalous acids from halides and hydrogen peroxide or oxygen, which form bioactive secondary metabolites of microbial origin with strong antibacterial and antifungal activities in follow-up reactions. Therefore, enzyme mimics and halogenating enzymes may be valuable tools to combat biofilm formation. Here, halogenating enzyme models are briefly described, enzyme mimics are classified according to their catalytic functions, and current knowledge about th…

chemistry.chemical_classificationMaterials science010405 organic chemistryMechanical EngineeringBiofilmHalogenation010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysisBiofoulingchemistry.chemical_compoundEnzymechemistryBiosynthesisMechanics of MaterialsHaloperoxidaseGeneral Materials ScienceHydrogen peroxideAdvanced Materials
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4-Vinylphthalic anhydride

1994

4-Vinylphthalic anhydride can be prepared from phthalic acid via bromination and subsequent olefination (Heck-reaction). Homo- and copolymerization with styrene was accomplished using AIBN as initiator. The copolymer compositions were determined by infrared-spectroscopy. The copolymerization parameters are rs=0,15 and rVPA=3,09, the corresponding Q, e values of 4-vinylphthalic anhydride are estimated as Q=3,34 and e=0.09.

chemistry.chemical_classificationPolymers and PlasticsRadical polymerizationHalogenationGeneral ChemistryPolymerCondensed Matter PhysicsStyrenechemistry.chemical_compoundPhthalic acidMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerGlass transitionPolymer Bulletin
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