Search results for "alkynylation"

showing 5 items of 15 documents

Highly enantioselective zinc/binol-catalyzed alkynylation of N-sulfonyl aldimines.

2008

chemistry.chemical_classificationSulfonylAldimineEnantioselective synthesischemistry.chemical_elementGeneral MedicineGeneral ChemistryZincCatalysisCatalysischemistryAlkynylationOrganic chemistryAmine gas treatingAngewandte Chemie (International ed. in English)
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ChemInform Abstract: Highly Enantioselective Copper(I)-Catalyzed Conjugate Addition of Terminal Alkynes to 1,1-Difluoro-1-(phenylsulfonyl)-3-en-2-one…

2014

A highly enantioselective copper-catalyzed conjugate alkynylation of monoactivated enones, namely 1,1-difluoro-1-(phenylsulfonyl)-3-en-2-ones, is described. The reaction products are obtained with good yields and excellent enantioselectivities (from 92 to 99% ee). The β-alkynylated difluoro(phenylsulfonyl) ketones can be converted into the corresponding β-alkynylated difluoro- and trifluoromethyl ketones, esters and amides. This is the first example on the use of 1,1-difluoro-1-(phenylsulfonyl)-3-en-2-ones as substrates in an enantioselective reaction, which have been shown to be new ester/amide surrogates.

chemistry.chemical_compoundTrifluoromethylAlkynylationChemistryAmideEnantioselective synthesischemistry.chemical_elementGeneral MedicineMedicinal chemistryCopperCatalysisConjugateChemInform
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ChemInform Abstract: Catalytic Enantioselective Conjugate Alkynylation of α,β-Unsaturated 1,1,1-Trifluoromethyl Ketones with Terminal Alkynes.

2016

Financial support (Grant CTQ2013-47494-P) from the Ministerio de Economia y Competitividad (MINECO-Gobierno de Espana). A.S.M. thanks the MINECO for a predoctoral grant (FPI program). Access to NMR and MS facilities from the Servei Central de Suport a la Investigacio Experimental (SCSIE)-UV is also acknowledged.

chemistry.chemical_compoundTrifluoromethylchemistryAlkynylationStereochemistryEnantioselective synthesisGeneral MedicineCatalysisConjugateChemInform
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ChemInform Abstract: Catalytic Asymmetric Conjugate Addition of Terminal Alkynes to β-Trifluoromethyl α,β-Enones.

2014

The first enantioselective conjugate alkynylation of β-trifluoromethyl α,β-enones (II) using terminal alkynes (I) and a taniaphos-Cu(I) complex as catalyst is described.

chemistry.chemical_compoundTrifluoromethylchemistryAlkynylationTerminal (electronics)StereochemistryEnantioselective synthesisGeneral MedicineCatalysisConjugateChemInform
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The first catalytic method for Heck alkynylation of unactivated aryl bromides (copper-free Sonogashira) in an ionic liquid: 1 mol-percent palladium/t…

2007

Herein we report the studies of Heck alkynylation (copper-free Sonogashira) with aryl halides (I, Br, Cl) employing various metallic precursors, tertiary phosphanes and bases in [BMIM][BF4] as the solvent. As a result, we provide the first method that allows the coupling of a large array of substrates, either activated or deactivated bromides in an ionic liquid. Furthermore, the system of highest efficiency is unexpectedly the simplest and cheaper combination that employs [Pd(η3-C3H5)Cl]2/PPh3 at only a 1 mol-% loading with pyrrolidine as the base and in the absence of a copper salt. The coupling of sterically and electronically deactivated bromides bearing different functional groups to ar…

copper-free SonogashiraIonic bondingchemistry.chemical_elementSonogashira coupling010402 general chemistry01 natural sciences7. Clean energyHeck alkynylationPyrrolidineCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactiontriphenylphosphaneOrganic chemistryPhysical and Theoretical ChemistryAlkylComputingMilieux_MISCELLANEOUSionic liquidchemistry.chemical_classificationcatalysis010405 organic chemistryArylOrganic ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistrymethylimidazolium0104 chemical sciencesSolventchemistryIonic liquidPalladium
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