Search results for "TRIF"

showing 10 items of 1419 documents

The introduction of fluorine atoms or trifluoromethyl groups in short cationic peptides enhances their antimicrobial activity

2006

The effect of introducing fluorine atoms or trifluoromethyl groups in either the peptidic chain or the C-terminal end of cationic pentapeptides is reported. Three series of amide and ester peptides were synthesised and their antimicrobial properties evaluated. An enhanced activity was found in those derivatives whose structure contained fluorine, suggesting an increase in their hydrophobicity.

StereochemistryClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementPeptideMicrobial Sensitivity TestsBiochemistryChemical synthesisMedicinal chemistryStructure-Activity Relationshipchemistry.chemical_compoundCationsAmideBenzyl CompoundsDrug DiscoveryHumansMolecular Biologychemistry.chemical_classificationTrifluoromethylMolecular StructureOrganic ChemistryCationic polymerizationStereoisomerismBiological activityFluorineAnti-Bacterial AgentsEukaryotic CellschemistryDrug DesignLipophilicityFluorineMolecular MedicineHydrophobic and Hydrophilic InteractionsOligopeptidesBioorganic & Medicinal Chemistry
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Simultaneous substitution of bridging acetate groups and reversible RhC bond cleavage in [Rh2(O2CCH3)3-{(C6H4)PPh2}(HO2CCH3)2] in the presence of CF…

1993

Abstract The reaction of the monometallated compound [Rh2(O2CCH3)3 {(C6H4)PPh2}(HO2CCH3)2] (1) with CF3CO2H at room temperature yields [Rh2(O2CCF3)3{(C6H4)PPh2}(HO2CCF3)2] (3) as the only isolable product. Compound 3 has been characterized by X-ray methods. 3 crystallizes in the space group P21 / n. It contains three trifluoroacetate groups bridging a Rh4+2 unit with a RhRh bond distance of 2.438(1) Ă; the fourth bridging ligand is a triphenylphosphine metallated at one of the ortho positions. Two molecules of trifluoroacetic acid occupy the axial coordination positions. In addition to the substitution of acetate groups, reversible electrophilic RhC bond activation is observed.

StereochemistryOrganic ChemistryBridging ligandCrystal structureBiochemistryInorganic ChemistryBond lengthchemistry.chemical_compoundCrystallographychemistryElectrophileMaterials ChemistryTrifluoroacetic acidCarboxylatePhysical and Theoretical ChemistryTriphenylphosphineBond cleavageJournal of Organometallic Chemistry
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Synthesis of tritiated derivatives of the diphenylether herbicides acifluorfen and acifluorfen methyl

1992

Acifluorfen 1 and acifluorfen methyl 2, two herbicides of the diphenylether family, are inhibitors of protoporphyrinogen oxidases. Two tritiated derivatives of these compounds, namely 3-[3H]-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid [3H]-1, and methyl 3-[3H]-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid [3H]-2, have been synthesised from 3-[3H]-5-hydroxybenzoic acid, in order to probe their interactions with the target enzymes.

Stereochemistry[SDV]Life Sciences [q-bio]Nitro compoundEtherAcifluorfenBiochemistryAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundMALHERBOLOGIEDrug DiscoveryPIPHENYL ETHERRadiology Nuclear Medicine and imagingSYNTHESESpectroscopyComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classification0303 health sciencesTrifluoromethyl030302 biochemistry & molecular biologyOrganic Chemistry3. Good health[SDV] Life Sciences [q-bio]Enzyme inhibitionEnzymeAcifluorfen-methylchemistryProtoporphyrinogen oxidaseCHIMIE ORGANIQUE
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Self-assembly of 1D- and 3D-networks through non-coordination intermolecular forces: synthesis and crystal structures of copper(I) complexes based on…

2007

Reaction of [Cu2(H3CCN)2(μ-pydz)3][PF6]2 (1) with an excess of pyridazine or phthalazine yielded the novel dinuclear complexes [Cu2(μ-pydz)3(pydz)2][PF6]2 (2) and [Cu2 (μ- pydz)(μ-phtz)2(phtz)2][PF6]2 (5), respectively. Depolymerisation of the coordination polymer 1 ∞ {[Cu(μ-pydz)2][PF6]} (3) in dichloromethane by addition of an excess of benzo[c]cinnoline afforded the dinuclear copper(I) salt [Cu2(μ-pydz)2(pydz)2(benzo[c]cinnoline)2][PF6]2 (4). Furthermore, a new route for the preparation of bis(benzonitrile)tris(μ-phthalazine)dicopper(I) bis(trifluoromethanesulfonate), [Cu2(C6H5CN)2(μ-phtz)3][CF3SO3]2 (7), was established from {[Cu(CF3SO3)]2 ・C6H5Me}, phthalazine and benzonitrile via the …

Stereochemistrychemistry.chemical_elementphthalazineCrystal structure010402 general chemistry01 natural sciencesPyridazinechemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistryCinnolineComputingMilieux_MISCELLANEOUS010405 organic chemistryIntermolecular force[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral Chemistrybenzo[c]cinnolineself-assemblyCopper0104 chemical sciencescopper(I)CrystallographyBenzonitrilepyridazinechemistryPhthalazineTrifluoromethanesulfonate
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The role of fluorine in the stereoselective tandem Aza-Michael addition to acrylamide acceptors: An experimental and theoretical mechanistic study

2007

Aza-Michael additions of alpha-amino esters to fluorinated acceptors take place in a highly stereoselective manner, to give partially modified Psi-[NHCH2]retropeptides incorporating a hydrolytically stable trifluoroalanine mimic. The reaction mechanism has been investigated experimentally and theoretically, in order to explain the effect of the trifluoromethyl group on the reactivity and the origins of the experimentally observed stereocontrol. The reaction is a two-step process, involving a tandem aza-Michael addition followed by a stereoselective hydrogen transfer. Both steps are base-catalyzed. The high level of stereocontrol is the result of a combination of electrostatic interactions a…

Steric effectsModels MolecularReaction mechanismMagnetic Resonance SpectroscopyStereochemistrychemistry.chemical_elementStereoisomerismCatalysisMass Spectrometrychemistry.chemical_compoundComputational chemistrycalculationsReactivity (chemistry)density functionalAcrylamideTrifluoromethyldiastereoselectivity fluorine chemistryOrganic ChemistryStereoisomerismGeneral ChemistryFluorinechemistryFluorineMichael reactionpeptidesStereoselectivityMichael reaction
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Palladium-Catalysed CH Bond Electrophilic Fluorination of Highly Substituted Arylpyrazoles: Experimental and DFT Mechanistic Insights

2015

A general protocol for palladium-catalysed CH mono- and di-fluorination of highly substituted arylpyrazoles is reported. Coupling pathways and substrate limitations are discussed in the light of complementary mechanistic experimental and density functional theory (DFT) studies. The mono- and di-ortho-fluorination of arylpyrazoles having substituted pyrazole groups and ortho-, meta-, or para-substituted arene moieties is achieved. Various pyrazole groups can efficiently promote the direct CH activation/fluorination of substrates bearing valuable reactive ester, cyano, halide and nitro functions. The presence of methoxy, methyl and trifluoromethyl is tolerated on the pyrazole directing groups…

Steric effectsTrifluoromethylElectrophilic fluorinationSubstituentchemistry.chemical_elementGeneral ChemistryPyrazoleOxidative additionMedicinal chemistrychemistry.chemical_compoundchemistryNitroOrganic chemistryPalladiumAdvanced Synthesis & Catalysis
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Stacking of Sterically Congested Trifluoromethylated Aromatics in their Crystals – The Role of Weak F···π or F···F Contacts

2020

European journal of organic chemistry : EurJOC 2020(38), 6073-6077 (2020). doi:10.1002/ejoc.202001008

Steric effectsaromaattiset yhdisteetChemistryOrganic ChemistryStackingstacking interactionskiteet540fluoriCrystallographyddc:540solid-state structurescrystalssupramolekulaarinen kemiafluorinated compoundsPhysical and Theoretical Chemistryröntgenkristallografiatrifluoromethyl substituents
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Intramolecular Nitrone Cycloaddition of α-(Trifluoromethyl)styrenes. Role of the CF3 Group in the Regioselectivity

2017

The intramolecular 1,3-dipolar cycloaddition of ortho-substituted 1,1,1-trifluoromethylstyrene-derived nitrones is described. Tricyclic fused isoxazolidines were obtained as major or exclusive products, in contrast to the case for nonfluorinated substrates, which rendered the bridged derivatives. This change in the regioselectivity was attributed to the electronic and, particularly, steric requirements of the trifluoromethyl group in comparison to the methyl group. It is worth mentioning that trifluoromethylstyrenes have been employed for the first time as dipolarophiles in a 1,3-dipolar intramolecular cycloaddition reaction, leading to the corresponding isoxazolidines bearing a quaternary …

Steric effectschemistry.chemical_classificationTrifluoromethylBicyclic molecule010405 organic chemistryStereochemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesCycloaddition0104 chemical sciencesNitronechemistry.chemical_compoundchemistryIntramolecular forceMoietyThe Journal of Organic Chemistry
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Bone Marrow Derived Mesenchymal Cells Secrete Granulopoietic Cytokines upon Danger Signaling

2014

Abstract Granulopoietic homeostasis is regulated at steady-state to supply sufficient numbers of pooled and circulating neutrophils to maintain barrier function against commensal flora. In addition, upon pathogenic microbial challenge, an increased formation of neutrophils is induced, termed ‘emergency granulopoiesis’. Antibody-mediated reduction of neutrophil numbers in steady-state induces a feedback loop leading to an increase of bone marrow granulopoiesis with expansion of hematopoetic stem and progenitor cells. This feedback loop was demonstrated to depend on TLR4 and TRIF, but not MyD88 signaling (Bugl et al. Blood 2013). In contrast, emergency granulopoiesis was shown to be dependent…

Stromal cellImmunologyMesenchymal stem cellInflammasomeCell BiologyHematologyBiologyBiochemistryGranulopoiesisCell biologyHaematopoiesismedicine.anatomical_structureTRIFImmunologymedicineBone marrowProgenitor cellmedicine.drugBlood
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On the Reaction of 3-Bromo-2-nitrobenzo[b]thiophene 13C-Labeled at C-2 with 3-(Trifluoromethyl)aniline:  A Preliminary Insight into a Nucleophilic Su…

1997

The results of the title reaction have furnished proofs against a rearrangement of the carbon-atom skeleton and for a nitro group shift in the relevant nucleophilic substitution.

Substitution reactionTrifluoromethylStereochemistryKornblum–DeLaMare rearrangementfungiOrganic Chemistrybehavioral disciplines and activitiesbody regionschemistry.chemical_compoundchemistryNucleophilic aromatic substitutionparasitic diseasesNitroNucleophilic substitutionThiopheneAcid hydrolysisThe Journal of Organic Chemistry
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