Search results for "Concerted reaction"

showing 6 items of 16 documents

Understanding the Nature of the Molecular Mechanisms Associated with the Competitive Lewis Acid Catalyzed[4+2] and[4+3] Cycloadditions between Arylid…

2004

The molecular mechanisms of the reactions between aryliden-5(4H)-oxazolone 1, and cyclopentadiene (Cp), in presence of Lewis acid (LA) catalyst to obtain the corresponding [4+2] and [4+3] cycloadducts are examined through density functional theory (DFT) calculations at the B3LYP/6-31G* level. The activation effect of LA catalyst can be reached by two ways, that is, interaction of LA either with carbonyl or carboxyl oxygen atoms of 1 to render [4+2] or [4+3] cycloadducts. The endo and exo [4+2] cycloadducts are formed through a highly asynchronous concerted mechanism associated to a Michael-type addition of Cp to the beta-conjugated position of alpha,beta-unsaturated carbonyl framework of 1.…

Reaction mechanismCyclopentadieneConcerted reactionStereochemistryOrganic ChemistryGeneral ChemistryCatalysisCycloadditionAdductchemistry.chemical_compoundNucleophilechemistryCascade reactionLewis acids and basesChemistry - A European Journal
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Theoretical study of 1,3-dipolar cycloaddition reactions with inverse electron demand - A DFT study of the lewis acid catalyst and solvent effects in…

2000

The molecular mechanism for the inverse electron demand 1,3-dipolar cycloaddition of nitrones with vinyl ethers has been characterized using density functional theory methods with the B3LYP functional and the 6−31G* basis set. Relative rates, regioselectivity, endo/exo stereoselectivity, Lewis acid catalyst and solvent effects are analyzed and discussed. Four reactive channels associated with the formation of two pairs of diasteromeric regioisomers have been characterized. Analysis of the geometries of the corresponding transition structures shows that the reaction in the gas phase takes place by an asynchronous concerted mechanism. These 1,3-dipolar cycloadditions present a large ortho reg…

Steric effectschemistry.chemical_classificationConcerted reactionOrganic ChemistryPhotochemistryCycloadditionNitroneLewis acid catalysischemistryComputational chemistry13-Dipolar cycloadditionLewis acids and basesPhysical and Theoretical ChemistrySolvent effects
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Dehydrochlorination of Hexachlorocyclohexanes Catalyzed by the LinA Dehydrohalogenase. A QM/MM Study

2015

The elucidation of the catalytic role of LinA dehydrohalogenase in the degradation processes of hexachlorocyclohexane (HCH) isomers is extremely important to further studies on the bioremediation of HCH polluted areas. Herein, QM/MM free energy simulations are employed to provide the details of the dehydrochlorination reaction of two HCH isomers (γ and β). In particular, the role of the protonation state of one of the catalytic residues-His73-is explored. Based on our calculations, two distinct minimum free energy pathways (concerted and stepwise) were found for γ-HCH and β-HCH. The choice of the reaction channel for the dehydrochlorination reactions of γ- and β-HCH was shown to depend on t…

biologyProtonConcerted reactionStereochemistryHexachlorocyclohexaneActive siteProtonationSurfaces Coatings and FilmsCatalysisQM/MMchemistry.chemical_compoundchemistryComputational chemistryMaterials Chemistrybiology.proteinDegradation (geology)Physical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Influence of the Ligand of Palladium(0) Complexes on the Rate of the Oxidative Addition of Aryl and Activated Alkyl Bromides: Csp2 −Br versus Csp3 −B…

2017

Kinetic data by means of electrochemical techniques are used to characterize the reactivity of aryl bromides and activated alkyl bromides in oxidative addition to palladium(0) complexes generated from three precursors: Pd0(PPh3)4, {Pd0(dba)2 + 2 PPh3} and {Pd0(dba)2 + 2 P(o Tol)3} in DMF at 25 °C. It is established that, for the investigated substrates 1-6 and 7-11, the oxidative addition at the Csp3 Br bond is much faster than that at the Csp2 Br bond when the palladium(0) is ligated by two PPh3. This explains why the regioselectivity in Suzuki-Miyaura reactions performed from substrates bearing both Csp2 Br and Csp3 Br groups is in favour of the substitution at the Csp3 Br bond. It is in …

chemistry.chemical_classification010405 organic chemistryConcerted reactionLigandArylOrganic ChemistryRegioselectivitychemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryOxidative additionCatalysis0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryReactivity (chemistry)Physical and Theoretical ChemistryAlkylPalladiumChemCatChem
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Gold(I)-catalyzed intermolecular oxyarylation of alkynes: unexpected regiochemistry in the alkylation of arenes.

2009

The reaction between acetylenes and sulfoxides, studied as a test case for gold-catalyzed intermolecular addition, provides the oxyarylation compounds 3 in good yields. Unpredictably, in all cases a single regioisomer arising from the electrophilic aromatic alkylation at the position adjacent to the sulfur atom is obtained instead of the expected Friedel−Crafts regioisomer. A new concerted mechanism based on DFT calculations is proposed to account for the products in this intermolecular gold(I)-catalyzed reaction.

inorganic chemicalsConcerted reactionOrganic ChemistryIntermolecular forceRegioselectivitychemistry.chemical_elementAlkylationPhotochemistryBiochemistrySulfurCatalysischemistryComputational chemistryElectrophileStructural isomerPhysical and Theoretical ChemistryOrganic letters
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ChemInform Abstract: Gold(I)-Catalyzed Intermolecular Oxyarylation of Alkynes: Unexpected Regiochemistry in the Alkylation of Arenes.

2010

The reaction between acetylenes and sulfoxides, studied as a test case for gold-catalyzed intermolecular addition, provides the oxyarylation compounds 3 in good yields. Unpredictably, in all cases a single regioisomer arising from the electrophilic aromatic alkylation at the position adjacent to the sulfur atom is obtained instead of the expected Friedel−Crafts regioisomer. A new concerted mechanism based on DFT calculations is proposed to account for the products in this intermolecular gold(I)-catalyzed reaction.

inorganic chemicalschemistryConcerted reactionIntermolecular forceElectrophileStructural isomerchemistry.chemical_elementRegioselectivityGeneral MedicineAlkylationSulfurMedicinal chemistryCatalysisChemInform
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