Search results for "fluorine chemistry"

showing 7 items of 7 documents

Anionic-anionic asymmetric tandem reactions: one-pot synthesis of optically pure fluorinated indolines from 2-p-tolylsulfinyl alkylbenzenes.

2008

Anionsgamma-sulfinyl carbanionsIndolesTandemChemistryindolinesOne-pot synthesisasymmetric synthesisEnantioselective synthesisBenzeneStereoisomerismGeneral ChemistryGeneral MedicineFluorineCatalysisfluorine chemistrychemistry.chemical_compoundIndolineOrganic chemistryAlkylbenzenesAngewandte Chemie (International ed. in English)
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Diversity-Oriented Synthesis of Highly Functionalized Alicycles across Dipolar Cycloaddition/Metathesis Reaction

2021

AbstractThis Account gives an insight into the selective functionalization of some readily available commercial cyclodienes across simple chemical transformations into functionalized small-molecular scaffolds. The syntheses involved selective cycloadditions, followed by ring-opening metathesis (ROM) of the resulting azetidin-2-one derivatives or isoxazoline frameworks and selective cross metathesis (CM) by discrimination of the C=C bonds on the alkenylated heterocycles. The CM protocols have been described when investigated under various conditions with the purpose on exploring chemodifferentiation of the olefin bonds and a study on the access of the corresponding functionalized β-lactam or…

Chlorosulfonyl isocyanateOlefin fiberNitrile010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryOrganofluorine chemistryMetathesis01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundSalt metathesis reactionCycloalkeneSynlett
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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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Copper-catalyzed regioselective synthesis of (E)-β-fluorovinyl sulfones

2019

Organofluorine compounds are finding increasing application in a variety of fields such as pharmaceutical, agrochemical, and material sciences. However, given the scarcity of fluorine-containing natural products, advancement in this area depends almost entirely on the development of new synthetic methodologies. In this article, we present the synthesis of a series of previously undescribed (E)-&beta

Vinyl CompoundsPharmaceutical Sciencealkynyl sulfonesChemical synthesisArticleCatalysisAnalytical ChemistrySulfonelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryorganofluorine chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistrycopper catalysisMolecular StructureOrganic ChemistryRegioselectivityFluorineHydrogen fluorideOrganofluorine chemistryβ-fluorovinyl sulfonechemistryChemistry (miscellaneous)regioselectivityCopper catalyzedMolecular MedicineOrganofluorine compoundshydrogenationCopper
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Asymmetric Synthesis of Fluorinated Monoterpenic Alkaloid Derivatives from Chiral Fluoroalkyl Aldimines via the Pauson‐Khand Reaction

2020

chemistry.chemical_classificationAldiminechemistry.chemical_compoundchemistryPauson–Khand reactionAlkaloidEnantioselective synthesisOrganic chemistryGeneral ChemistryN-tert-butanesulfinyl imineOrganofluorine chemistryAdvanced Synthesis & Catalysis
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Novel Stereoselective Intramolecular Processes for the Generation of New Molecular Entities

2019

La Química Orgánica, además de constituir una fuente inagotable de fascinación académica por su capacidad de generar un número virtualmente infinito de nuevas estructuras moleculares, ha proporcionado una poderosa herramienta, el cribado de librerías de moléculas orgánicas, en el ámbito de la química biológica/médica y el descubrimiento de fármacos que se ha convertido en el caballo de batalla en la identificación de nuevas dianas terapéuticas y sus correspondientes moduladores y potenciales fármacos, con un impacto directo sobre la salud humana. La principal problemática de estas librerías es el aspecto de la diversidad estructural, ya que la probabilidad de dar con un fármaco candidato es…

organofluorine chemistry:QUÍMICA::Química orgánica [UNESCO]organocatalysisUNESCO::QUÍMICA::Química orgánicaquímica orgánicaorganic chemistry
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New methodologies in transition metal catalysis. Organofluorine chemistry as the benchmark application.

2017

A lo largo de las últimas décadas, los compuestos organofluorados han encontrado numerosas aplicaciones dentro del campo de las industrias farmacéutica y agroquímica, así como en ciencias de los materiales. Dadas las singulares propiedades del átomo de flúor, éste es capaz de inducir alteraciones significativas en propiedades físico-químicas de las moléculas como lipofilia, distribución de cargas, acidez-basicidad, capacidad de formar enlaces de hidrógeno e incluso, equilibrios conformacionales. Sin embargo, la presencia de flúor en productos naturales es escasa. De hecho, la gran mayoría de las moléculas orgánicas que contienen flúor son sintéticas. De ahí el gran interés por parte de la c…

transition metal catalysisUNESCO::QUÍMICAorganofluorine chemistrymetathesispalladium catalysis:QUÍMICA [UNESCO]gold catalysis
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