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showing 10 items of 1967 documents

Lewis Acid Mediated Domino Reaction between 2-Cyclohexenone and Methyl Azide - A DFT Study

2005

We have studied the Lewis acid mediated domino reaction between 2-cyclohexenone and methyl azide at the B3LYP/6-31G* and B3LYP/6-31+G**//B3LYP/6-31G* levels of theory. A complete survey of the potential energy surface is presented, and the structures of the stationary points and the corresponding molecular mechanism are discussed. The calculations suggest that the product, a cyclopentanone derivative, is formed by means of a domino process that comprises three consecutive reactions. The first and rate-limiting step is a concerted 1,3-dipolar cycloaddition between the Lewis acid coordinated cyclohexenone and methyl azide that yields the corresponding bicyclic 1,2,3-triazoline. The second rea…

StereochemistryOrganic ChemistryCyclopentanonePolarizable continuum modelMedicinal chemistryTautomerCycloadditionchemistry.chemical_compoundchemistryCascade reactionCyclohexenoneLewis acids and basesPhysical and Theoretical ChemistryMethyl azideEuropean Journal of Organic Chemistry
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A density functional theory study of the regio- and stereoselectivity of the 1,3-dipolar cycloaddition of C-methyl substituted pyrazinium-3-olates wi…

2013

Abstract A DFT [B3LYP/6-31G(d)] study was carried out on the 1,3-dipolar cycloaddition (13DC) reactions of multi C-methyl substituted pyrazinium-3-olates with methyl acrylate (MA) and methyl methacrylate (MMA). Thermodynamic and kinetic parameters of the possible endo/exo stereoisomeric and 6-ester/7-ester regioisomeric pathways have been determined. The skeleton rearrangement of the 6-exo [3 + 2] cycloadducts into the [4 + 2] adducts is also considered. The electrophilic, P k + , and nucleophilic, P k - , Parr functions are used to have better understanding of the regioselectivity of these 13DC reactions. In all cases the exo pathways are more favourable compared to the endo alternatives. …

StereochemistryRegioselectivityCondensed Matter PhysicsBiochemistryCycloadditionchemistry.chemical_compoundchemistryNucleophileElectrophile13-Dipolar cycloadditionStereoselectivityPhysical and Theoretical ChemistryMethyl methacrylateMethyl acrylateComputational and Theoretical Chemistry
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Control of N-Heterocyclic Carbene Catalyzed Reactions of Enals: Asymmetric Synthesis of Oxindole-γ-Amino Acid Derivatives.

2017

A strategy to control the switch between a non‐cycloaddition reaction and a cycloaddition reaction of enals, using N‐heterocyclic carbene (NHC) catalyisis, has been developed. The new scalable protocol leads to γ‐amino‐acid esters bearing a tetrasubstituted stereocenter in good yields and high stereoselectivities by homo‐Mannich reactions of enals and isatin‐derived ketimines. By simply changing the N‐ketimine substituent to an ortho‐hydroxy phenyl group, the corresponding spirocyclic oxindolo‐γ‐lactams are obtained. peerReviewed

StereochemistrySubstituent010402 general chemistry01 natural sciencesCatalysisStereocenterCatalysischemistry.chemical_compoundaldehyditaldehydesPhenyl groupOxindoleta116orgaaniset yhdisteetkemiallinen synteesi010405 organic chemistryEnantioselective synthesisGeneral MedicineGeneral ChemistryCycloaddition0104 chemical scienceschemistryorganic compoundsCarbenechemical synthesisAngewandte Chemie (International ed. in English)
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Understanding the molecular mechanism of the [3 + 2] cycloaddition reaction of benzonitrile oxide toward electron-richN-vinylpyrrole: a DFT study

2016

The [3 + 2] cycloaddition (32CA) reaction of benzonitrile oxide, BNO 2, with an electron-rich N-vinylpyrrole derivative, NVP 3a, in the presence of dichloromethane, has been theoretically studied using density functional theory (DFT) methods at the B3LYP/6-31G(d) level. This 32CA reaction presents a relatively high activation Gibbs free energy as a result of the low polar character of this zwitterionic-type (zw-type) reaction. Analyses of the calculated relative Gibbs free energies and transition state geometries indicate that the studied 32CA reaction, in excellent agreement with experimental outcomes, takes place in a complete regioselective manner as a consequence of the steric repulsion…

Steric effects010405 organic chemistryOrganic Chemistry010402 general chemistry01 natural sciencesCycloadditionElectron localization function0104 chemical sciencesGibbs free energysymbols.namesakechemistry.chemical_compoundBenzonitrilechemistryComputational chemistrysymbolsSingle bondDensity functional theoryPhysical and Theoretical ChemistryDerivative (chemistry)Journal of Physical Organic Chemistry
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Photochemical Generation of Cyclophanes from 1,3,5-Trisubstituted Benzenes with Chalcone Chromophores

2007

(E,E,E)-1,3,5-Tricinnamoylbenzene (7a) photodimerizes in solution to the [4.4.4](1,3,5)cyclophane 8a. The process consists of three consecutive steps in which cisoid enone conformations of 7a react in regio- and stereoselective anti-head-to-head cycloadditions. (E,E,E)-1,3,5-Tris(3-oxo-3-phenylpropenyl)benzene (13a), an isomer of 7 with reversed enone units, shows a single [2π+2π] cycloaddition of the same type. Due to steric reasons, it is afterwards not capable of intramolecular processes and oligomerizes by intermolecular photocycloadditions. Photolyses in the crystalline state yield dimers by topochemically controlled syn-head-to-tail processes (7a → 10a, 13a → 15a). An efficient dimeri…

Steric effectsChalconeOlefin fiberChemistryStereochemistryOrganic ChemistryRegioselectivityPhotochemistryCycloadditionchemistry.chemical_compoundIntramolecular forcePhysical and Theoretical ChemistryEnoneCyclophaneEuropean Journal of Organic Chemistry
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Steric interactions controlling the syn diastereofacial selectivity in the [3 + 2] cycloaddition reaction between acetonitrile oxide and 7-oxanorborn…

2017

A Molecular Electron Density Theory study of the zw-type 32CA reactions of acetonitrile oxide (NO) with two 7-oxanorborn-5-en-2-ones (ONBs) has been performed at the DFT B3LYP/6-31G(d) computational level. These cycloadditions proceed through one-step mechanisms with high activation energies and present low para regio and complete syn diastereofacial selectivities. While the non-polar character of these zw-type 32CA reactions, which is the consequence of the insufficient electrophilic activation of ONBs, according to the analysis of the conceptual DFT reactivity indices, accounts for the high activation energies, and low para regioselectivity, NCI topological analyses at the anti/syn pairs …

Steric effectsElectron density010405 organic chemistryStereochemistryChemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesCycloaddition0104 chemical sciencesAcetonitrile oxideComputational chemistryElectrophileReactivity (chemistry)Physical and Theoretical ChemistrySelectivityJournal of Physical Organic Chemistry
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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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Comparison of linear and hyperbranched polyether lipids for liposome shielding by 18F-radiolabeling and positron emission tomography

2018

Multifunctional and highly biocompatible polyether structures play a key role in shielding liposomes from degradation in the bloodstream, providing also multiple functional groups for further attachment of targeting moieties. In this work hyperbranched polyglycerol (hbPG) bearing lipids with long alkyl chain anchor are evaluated with respect to steric stabilization of liposomes. The branched polyether lipids possess a hydrophobic bis(hexadecyl)glycerol membrane anchor for the liposomal membrane. hbPG was chosen as a multifunctional alternative to PEG, enabling the eventual linkage of multiple targeting vectors. Different hbPG lipids (Mn = 2900 and 5200 g mol-1) were examined. A linear bis(h…

Steric effectschemistry.chemical_classificationLiposomePolymers and PlasticsChemistryBioengineering02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical sciencesBiomaterialsMembranePEG ratioMaterials ChemistryAlkoxy grouplipids (amino acids peptides and proteins)0210 nano-technologyAlkyl
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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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Dynamics analysis of distributed parameter system subjected to a moving oscillator with random mass, velocity and acceleration

2002

Abstract The problem of calculating the response of a distributed parameter system excited by a moving oscillator with random mass, velocity and acceleration is investigated. The system response is a stochastic process although its characteristics are assumed to be deterministic. In this paper, the distributed parameter system is assumed as a beam with Bernoulli–Euler type analytical behaviour. By adopting the Galerkin's method, a set of approximate governing equations of motion possessing time-dependent uncertain coefficients and forcing function is obtained. The statistical characteristics of the deflection of the beam are computed by using an improved perturbation approach with respect t…

Stochastic processMechanical EngineeringMonte Carlo methodMathematical analysisAerospace EngineeringPerturbation (astronomy)Equations of motionMoving loadOcean EngineeringStatistical and Nonlinear PhysicsCondensed Matter PhysicsClassical mechanicsNuclear Energy and EngineeringDistributed parameter systemRandom vibrationGalerkin methodCivil and Structural EngineeringMathematicsProbabilistic Engineering Mechanics
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