Search results for "nucleophile"

showing 10 items of 385 documents

Unexplored nucleophilic ring opening of aziridines.

2010

The reactivity of dianions of carboxylic acids towards aziridines has been studied. Although, a similar reactivity to that of enolates from ketones, esters or amides has been observed, the method directly yields g-aminoacids in one step. The method is complementary of previous results of enenediolate reactivity with other electrophiles. A comparative study with the reactivity of this enediolates with epoxides is included.

enediolatePharmaceutical ScienceRing (chemistry)ArticleAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryNucleophileDrug DiscoveryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryAmino AcidsChemistryOrganic Chemistryγ-aminoacidsRegioselectivityg-aminoacidsKetonesdiastereoselectivityChemistry (miscellaneous)aziridinesregioselectivityElectrophileMolecular MedicineEpoxy CompoundsMolecules (Basel, Switzerland)
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Rearrangements of 1,2,4-Oxadiazole: “One Ring to Rule Them All”

2017

[Figure not available: see fulltext.] 1,2,4-Oxadiazoles are heterocycles characterized by low aromaticity and the presence of a weak O–N bond and are widely studied due to their tendency to rearrange into more stable heterocyclic compounds. This review covers literature from the last fifteen years, highlighting the general features of 1,2,4-oxadiazoles and their applications. Regarding the reactivity, the development of classical reactions (thermal and photochemical rearrangements) is presented in terms of synthetic utility and mechanistic insight. Among the relevant rearrangement reactions, the Boulton–Katritzky Rearrangement (BKR), Migration – Nucleophilic Attack – Cyclization (MN…

heterocyclic rearrangementphotochemistry010405 organic chemistryOrganic Chemistry124-oxadiazoleOxadiazoleBoulton–Katritzky rearrangementAromaticitySettore CHIM/06 - Chimica Organica010402 general chemistryRing (chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryComputational chemistryANRORCReactivity (chemistry)Chemistry of Heterocyclic Compounds
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Structural Origin of Metal Specificity in Isatin Hydrolase from Labrenzia aggregata Investigated by Computer Simulations.

2017

We performed quantum-chemical calculations, ab initio molecular dynamics, hybrid quantum mechanics/molecular mechanics (QM/MM) and enhanced sampling metadynamics simulations to investigate the origin of metal specificity in isatin hydrolase from Labrenzia aggregata. The peculiar octahedral binding geometry of the Mn2+ ion in the Michaelis complex includes both the isatin substrate and the catalytic water within the first coordination shell of the cation. Our calculations show that the same arrangement of the ligands cannot be efficiently achieved in the presence of other small divalent metal cations such as Zn2+ or Cu2+ . On the contrary, bulkier alkaline-earth cations such as Mg2+ , which …

inorganic chemicals0301 basic medicineIsatinCations DivalentHydrolasesMolecular Dynamics SimulationLigands01 natural sciencesCatalysisQM/MMMetal03 medical and health sciencesMolecular dynamicschemistry.chemical_compoundNucleophileBacterial Proteins0103 physical sciencesHydrolaseMoietyComputer SimulationRhodobacteraceae010306 general physicsIsatinOrganic ChemistryMetadynamicsWaterGeneral ChemistryCrystallography030104 developmental biologychemistryMetalsvisual_artvisual_art.visual_art_mediumQuantum TheoryThermodynamicsProtein BindingChemistry (Weinheim an der Bergstrasse, Germany)
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A kinetic study of the basic hydrolysis of 2-phenylethyl nitrite in the presence of borate buffer and β-cyclodextrin

2002

The kinetics of the hydrolysis of 2-phenylethyl nitrite have been studied in basic aqueous solutions (borate buffer) in the absence and presence of β-cyclodextrin. The observed kinetic trends show that the hydrolysis reaction consists of at least three subsequent processes. The first is a fast acid-base reaction between the boron atom of boric acid and oxygen atom of the alkyl nitrite. The second one should be the nucleophilic attack of hydroxyl ion on the alkyl nitrite. The last process could be referred to as a combination of transfer of hydrogen acid to a water molecule followed by ruptures of nitrogen-oxygen and boron-oxygen bonds. The effect of β- cyclodextrin on each process is also d…

inorganic chemicalschemistry.chemical_classificationAqueous solutionCyclodextrinOrganic ChemistryKineticsInorganic chemistryMedicinal chemistrylcsh:QD241-441Boric acidchemistry.chemical_compoundHydrolysislcsh:Organic chemistryNucleophilechemistryNitriteAlkylArkivoc
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A DFT study on the NHC catalysed Michael addition of enols to α,β-unsaturated acyl-azoliums. A base catalysed C–C bond-formation step

2013

The NHC catalysed nucleophilic additions of enols to α,β-unsaturated acyl-azolium intermediates have been investigated using DFT methods at the MPWB1K/6-31G** computational level. In the direct and the conjugate additions, formation of a hydrogen bond (HB) with the carboxyl oxygen is not sufficient to favour the C-C bond formation as a consequence of the low nucleophilic character of enols. Interestingly, when enols form a HB with the chloride counterion, the activation energies associated with the conjugate addition decrease as a consequence of the increased nucleophilic character of enols and the increased electrophilic character of the 'acyl-azolium + Cl' ion pair. Analysis of the DFT re…

inorganic chemicalschemistry.chemical_classificationHydrogen bondChemistryStereochemistryOrganic ChemistryBiochemistryChlorideMedicinal chemistryNucleophileElectrophileMichael reactionmedicineReactivity (chemistry)Physical and Theoretical ChemistryCounterionmedicine.drugConjugateOrg. Biomol. Chem.
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Divergent reactivity of nucleophilic 1-bora-7a-azaindenide anions

2017

The reactions of 1-bora-7a-azaindenide anions, prepared in moderate to excellent yields by reduction of the appropriate 1-bora-7a-azaindenyl chlorides with KC8 in THF, with alkyl halides and carbon dioxide were studied. With alkyl halides (CH2Cl2, CH3I and BrCH(D)CH(D)tBu), the anions behave as boron anions, alkylating the boron centre via a classic SN2 mechanism. This was established with DFT methods and via experiments utilizing the neo-hexyl stereoprobe BrCH(D)CH(D)tBu. These reactions were in part driven by a re-aromatization of the six membered pyridyl ring upon formation of the product. Conversely, in the reaction of the 1-bora-7a-azaindenide anions with CO2, a novel carboxylation of …

inorganic chemicalschemistry.chemical_classificationanionit010405 organic chemistryHalidechemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryNucleophilechemistryCarboxylation13. Climate actionbooriSN2 reactionReactivity (chemistry)Boronboronta116anionsAlkyl
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Can the absence of solvation of neutral reagents by ionic liquids be responsible for the high reactivity in base-assisted intramolecular nucleophilic…

2005

[reaction: see text] The kinetics of the rearrangement of the Z-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1a) into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (2a) induced by amines have been studied in two room-temperature ionic liquids (IL-1, [BMIM][BF4] and IL-2, [BMIM][PF6]). The data collected show that the reaction occurs faster in ionic liquids than in other conventional solvents previously studied (both polar or apolar, protic or aprotic). Presumably, this could depend on their peculiar ability to minimize the strong substrate-solvent, amine-solvent and amine-amine interactions occurring in conventional solvents.

ionic liquids mononuclear rearrangement of heterocycles base catalysisOrganic ChemistrySolvationSolventchemistry.chemical_compoundchemistryNucleophileComputational chemistryIntramolecular forceIonic liquidNucleophilic substitutionOrganic chemistryReactivity (chemistry)Solvent effects
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Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence.

2017

A study exploring the chemical behavior of some dihydroxylated β-amino ester stereo- and regioisomers, derived from unsaturated cyclic β-amino acids is described. The nucleophilic fluorinations involving hydroxy–fluorine exchange of some highly functionalized alicyclic diol derivatives have been carried out in view of selective fluorination, investigating substrate dependence, neighboring group assistance and chemodifferentiation.

isomeriaDiolchemistry.chemical_elementaminohapot010402 general chemistry01 natural sciencesFull Research Paperlcsh:QD241-441chemistry.chemical_compoundAlicyclic compoundNucleophilelcsh:Organic chemistryfluorineStructural isomerOrganic chemistrystereoisomersChemoselectivitylcsh:Scienceta116chemistry.chemical_classificationamino acids010405 organic chemistryOrganic ChemistrySubstrate (chemistry)03.01. Általános orvostudományfluori0104 chemical sciencesChemistrychemistrychemoselectivityFluorineSurface modificationfunctionalizationlcsh:QBeilstein journal of organic chemistry
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Convergent results from experimental and theoretical DFT studies of the intramolecular rearrangement of Z-hydrazones of 3-acetyl-1,2,4-oxadiazoles

2004

A combined kinetic and theoretical study of the monocyclic rearrangements of heterocycles (MRH) has been carried out. The interconversion of the Z-hydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole into the corresponding triazole has been experimentally investigated in dioxane/water in the pS(+) range 5.5(5)-13.9. The uncatalyzed region has been examined at the DFT level using a model system formed by the Z-hydrazone of 3-formyl-1,2,4-oxadiazole and one or two water molecules. The environmental effect of the solvent has been emulated using a continuum model (COSMO) approach. The kinetic data suggest a concerted process where the magnitude of the activation barrier is determined by the interpl…

ketonesTriazoleSettore CHIM/06 - Chimica OrganicaKinetic energyEnvironmental effectSolventchemistry.chemical_compoundchemistryNucleophileNitrogen atomComputational chemistryActivation barrierIntramolecular forceIntramolecular rearrangementMoleculePhysical and Theoretical ChemistryMRH
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Probing the Extremes of Covalency in M-Al bonds: Lithium and Zinc Aluminyl Compounds.

2022

Synthetic routes to lithium, magnesium, and zinc aluminyl complexes are reported, allowing for the first structural characterization of an unsupported lithium-aluminium bond. Crystallographic and quantum-chemical studies are consistent with the presence of a highly polar Li-Al interaction, characterized by a low bond order and relatively little charge transfer from Al to Li. Comparison with magnesium and zinc aluminyl systems reveals changes to both the M-Al bond and the (NON)Al fragment (where NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethylxanthene), consistent with a more covalent character, with the latter complex being shown to react with CO<sub>2</sub> vi…

low valent compoundssinkki (metallit)ChemistryMagnesiumaluminiumzincchemistry.chemical_elementkompleksiyhdisteetGeneral ChemistryZincGeneral MedicineBond orderCatalysiskemialliset sidoksetCrystallographylitiumNucleophilelithiumCovalent bondAluminiumaluminylPolarLithiumalumiiniAngewandte Chemie (International ed. in English)
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