Search results for "trifluoromethyl"

showing 10 items of 288 documents

Approaches for the introduction of fluorinated substituents into [1,2,3]Triazolo[1,5-a]pyridines

2014

Abstract [1,2,3]Triazolo[1,5-a]pyridines functionalization with a trifluoromethyl group has been achieved for the first time using different synthetic strategies. Furthermore, these scaffolds have been employed as starting material in the synthesis of new 2,6-disubstituted pyridines containing the trifluoromethyl group, compounds that are not available using other methodologies. A fluorine-mediated triazolopyridine dimerisation is described, improving the previously known synthetic method. Preliminary studies focused on exploring triazolopyridines reactivity with electrophilic fluorine have revealed a new approach for the obtainment of imidazopyridines.

TrifluoromethylOrganic Chemistrychemistry.chemical_elementBiochemistryCombinatorial chemistryInorganic Chemistrychemistry.chemical_compoundchemistryGroup (periodic table)ElectrophileFluorineEnvironmental ChemistrySurface modificationReactivity (chemistry)TriazolopyridinePhysical and Theoretical ChemistryJournal of Fluorine Chemistry
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Synthesis, X-ray Structure Determination, and Comprehensive Photochemical Characterization of (Trifluoromethyl)diazirine-Containing TRPML1 Ligands

2021

Potential (trifluoromethyl)diazirine-based TRPML1 ion channel ligands were designed and synthesized, and their structures were determined by single-crystal X-ray diffraction analysis. Photoactivation studies via 19F NMR spectroscopy and HPLC-MS analysis revealed distinct kinetical characteristics in selected solvents and favorable photochemical properties in an aqueous buffer. These photoactivatable TRPML activators represent useful and valuable tools for TRPML photoaffinity labeling combined with mass spectrometry.

TrifluoromethylPhotoaffinity labelingTRPML010405 organic chemistryX-RaysOrganic ChemistryX-rayPhotoaffinity LabelsLigands010402 general chemistryPhotochemistryMass spectrometry01 natural sciencesMass Spectrometry0104 chemical sciencesCharacterization (materials science)chemistry.chemical_compoundDiazomethanechemistry540 ChemistryDiazirine570 Life sciences; biologyIon channelThe Journal of Organic Chemistry
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Hyperfine couplings ofN-alkoxy-N-polynitrophenylaminyl radicals determined by ENDOR and TRIPLE resonance spectroscopy

1995

Lead tetraacetate one-electron oxidation of nine different N-alkoxy-2,6-dinitroanilines substituted with trifluoromethyl, methyl and nitro groups in position 4 yielded aminyl radicals for which hyperfine couplings were measured by ENDOR and TRIPLE resonance spectroscopy. The optimum temperature range for proton ENDOR and general TRIPLE resonance measurements of aminyl radicals was 210–250 K and for nitrogen ENDOR 260 K in toluene. Further lowering for the temperature rapidly decreased the EPR intensity. The concentration of the sample and the amount of oxidant were optimized for obtaining ENDOR spectra. The relative signs of the hyperfine couplings of nitrogens, fluorines and protons were d…

TrifluoromethylProtonRadicalGeneral ChemistryPhotochemistryResonance (chemistry)law.inventionchemistry.chemical_compoundchemistrylawAlkoxy groupPhysical chemistryGeneral Materials ScienceElectron paramagnetic resonanceSpectroscopyHyperfine structureMagnetic Resonance in Chemistry
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Influence of Remote Substituents on the Equatorial/Axial Selectivity in the Monooxygenation of Methylene C−H Bonds of Substituted Cyclohexanes

2001

The reactivity of individual C--H bonds in the methyl(trifluoromethyl)dioxirane TFDO oxygenation of stereogenic methylene groups in conformationally homogeneous monosubstituted cyclohexanes (2) has been determined. The unexpectedly high occurrence of O-atom insertion into C--H(ax) bonds suggests an in plane trajectory attack in the oxygenation while the diastereoselectivity of the reaction is qualitatively interpreted on the basis of the distinct hyperconjugative stabilization by the substituent of diastereomeric transition states due to long-range through bond interactions.

TrifluoromethylStereochemistrySubstituentGeneral ChemistryBiochemistryCatalysisTransition stateStereocenterchemistry.chemical_compoundColloid and Surface ChemistrychemistryDioxiraneCyclohexanesReactivity (chemistry)MethyleneJournal of the American Chemical Society
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ChemInform Abstract: Synthesis and Induction of G0-G1 Phase Arrest with Apoptosis of 3,5-Dimethyl-6-phenyl-8-(trifluoromethyl)-5,6-dihydropyrazolo[3,…

2009

The multistep synthesis of 3,5-dimethyl-6-phenyl-8-(trifluoromethyl)-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-one 15 has been carried out. The compound showed antiproliferative and apoptotic effects against K562, K562-R (imatinib mesilate resistant), HL60 and multidrug resistant (MDR) HL60 cell lines. Compound 15 showed a pro-apoptotic activity against HL60 and K562 resistant cell lines markedly higher than etoposide and busulfan, respectively. Flow cytometry studies carried out on K562 cells allowed to establish that 15 induces G0-G1 phase arrest followed by apoptosis.

Trifluoromethylmedicine.diagnostic_testHL60General MedicineMolecular biologyFlow cytometryMultiple drug resistancechemistry.chemical_compoundchemistryApoptosishemic and lymphatic diseasesmedicineBusulfanEtoposidemedicine.drugK562 cellsChemInform
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Low-temperature molecular layer deposition using monifunctional aromatic precursors and ozone-based ring-opening reactions

2017

Molecular layer deposition (MLD) is an increasingly used deposition technique for producing thin coatings consisting of purely organic or hybrid inorganic-organic materials. When organic materials are prepared, low deposition temperatures are often required to avoid decomposition, thus causing problems with low vapor pressure precursors. Monofunctional compounds have higher vapor pressures than traditional bi- or trifunctional MLD precursors, but do not offer the required functional groups for continuing the MLD growth in subsequent deposition cycles. In this study, we have used high vapor pressure monofunctional aromatic precursors in combination with ozone-triggered ring-opening reactions…

Vapor pressureHydrostatic pressure02 engineering and technologyphenols01 natural sciencesdepositionchemistry.chemical_compoundhybrid materialsElectrochemistryGeneral Materials Sciencecharacterizationinfrared spectroscopyta116Spectroscopyring opening reactionTrifluoromethylvapor pressurehybrid organic-inorganiclow-temperatureSurfaces and Interfacesself assembly021001 nanoscience & nanotechnologyCondensed Matter Physicsdecay (organic)hydrostatic pressure0210 nano-technologyHybrid materialLayer (electronics)Inorganic chemistryta221mechanismnegative ions010402 general chemistrycomplex mixturesinorganic coatingsBenzaldehydeAtomic layer depositionPhenolta216ta115ta114aromatic compoundsmonofunctional aromaticstemperature0104 chemical sciencesozonechemistryALDatomic layer depositionMLDLangmuir
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ChemInform Abstract: Synthesis of Functionalized Indoles with a Trifluoromethyl-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselect…

2010

Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

Zirconiumchemistry.chemical_compoundCarbon atomTrifluoromethylchemistryEnantioselective synthesischemistry.chemical_elementGeneral MedicineAlkylationMedicinal chemistryFriedel–Crafts reactionPyrrole derivativesStereocenterChemInform
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Perfluoroketene dithioacetals and perfluorodithiocarboxylic acid derivatives: Versatile tools for organofluorine synthesis

2007

Perfluoroketene dithioacetals are simple and versatile compounds that can be transformed into a large variety of trifluoromethyl derivatives, in particular aza- and thiaheterocycles, perhalodithiocrotonic esters, and fluorinated dithiol thiones. These unsaturated perfluorodithioesters and analogs give interesting polar cycloaddition reactions whose mechanism is strongly influenced by the fluorine substitution. This substitution plays an important role in the reactivity of saturated perfluorodithiocarboxylic acids as well. Except for the carbophilic addition of allyl Grignard reagents to perfluorocarboxamides, a domino thiophilic addition-fluoride elimination was the main reaction process. I…

[CHIM.MATE] Chemical Sciences/Material chemistryTrifluoromethyl010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistrychemistry.chemical_elementDithiolGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistry01 natural sciencesCombinatorial chemistryDominoCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionReagentFluorineOrganic chemistryReactivity (chemistry)ComputingMilieux_MISCELLANEOUS
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CCDC 1962572: Experimental Crystal Structure Determination

2022

Related Article: Ahmed F. Abdel-Magied, Yusuf Theibich, Amrendra K. Singh, Ahibur Rahaman, Isa Doverbratt, Arun K. Raha, Matti Haukka, Michael G. Richmond, Ebbe Nordlander|2020|Dalton Trans.|49|4244|doi:10.1039/C9DT04799A

bis(mu-hydrido)-(mu-sulfido)-(mu-(SS)-1-(2-(diphenylphosphino)phenyl)-2-(1-(bis(35-bis(trifluoromethyl)phenyl)phosphino)ethyl)ferrocene)-heptacarbonyl-tri-rutheniumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1962571: Experimental Crystal Structure Determination

2022

Related Article: Ahmed F. Abdel-Magied, Yusuf Theibich, Amrendra K. Singh, Ahibur Rahaman, Isa Doverbratt, Arun K. Raha, Matti Haukka, Michael G. Richmond, Ebbe Nordlander|2020|Dalton Trans.|49|4244|doi:10.1039/C9DT04799A

bis(mu-hydrido)-(mu-sulfido)-(mu-(SS)-1-(2-(diphenylphosphino)phenyl)-2-(1-(bis(35-bis(trifluoromethyl)phenyl)phosphino)ethyl)ferrocene)-heptacarbonyl-tri-rutheniumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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