Search results for "cascade [energy]"

showing 10 items of 55 documents

ChemInform Abstract: Asymmetric Synthesis of Cyclopentanes Bearing Four Contiguous Stereocenters via an NHC-Catalyzed Michael/Michael/Esterification …

2016

An NHC-catalyzed Michael/Michael/esterification domino reaction via homoenolate/enolate intermediates for the asymmetric synthesis of tetrasubstituted cyclopentanes bearing four contiguous stereocenters is described. A variety of α,β-unsaturated aldehydes and 2-nitroallylic acetates react well with good domino yields and high stereoselectivities.

CyclopentanesBearing (mechanical)Cascade reactionlawChemistryStereochemistryEnantioselective synthesisGeneral MedicineDominolaw.inventionCatalysisStereocenterChemInform
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Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.

2016

An NHC-catalyzed Michael/Michael/esterification domino reaction via homoenolate/enolate intermediates for the asymmetric synthesis of tetrasubstituted cyclopentanes is described.

CyclopentanesStereochemistry010402 general chemistry01 natural sciencesCatalysisDominoCatalysisStereocenterCascade reactiondomino reactionMaterials Chemistryta116cyclopentane motifs010405 organic chemistryChemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry5400104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemistryddc:540Ceramics and CompositesChemical communications (Cambridge, England)
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DNA-Based Enzyme Reactors and Systems

2016

During recent years, the possibility to create custom biocompatible nanoshapes using DNA as a building material has rapidly emerged. Further, these rationally designed DNA structures could be exploited in positioning pivotal molecules, such as enzymes, with nanometer-level precision. This feature could be used in the fabrication of artificial biochemical machinery that is able to mimic the complex reactions found in living cells. Currently, DNA-enzyme hybrids can be used to control (multi-enzyme) cascade reactions and to regulate the enzyme functions and the reaction pathways. Moreover, sophisticated DNA structures can be utilized in encapsulating active enzymes and delivering the molecular…

DNA sensorsGeneral Chemical EngineeringeducationNanotechnologyDNA nanodevice02 engineering and technologyReviewBiology010402 general chemistry01 natural scienceslcsh:Chemistrychemistry.chemical_compoundDna nanostructuresDNA nanotechnologyDNA origamiGeneral Materials ScienceDNA nanotechnologychemistry.chemical_classificationPhysicsfood and beveragesself-assemblycascade reactions021001 nanoscience & nanotechnologyBiocompatible materialnanolääketiedenanomedicineDrug-deliveryMaterials science0104 chemical sciencesdrug-deliveryChemistryenzymeEnzymechemistrylcsh:QD1-999drug deliveryNanomedicineDNA origami0210 nano-technologyDNABiotechnologyNanomaterials
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Mechanistic details of the domino reaction of nitronaphthalenes with the electron-rich dienes. A DFT study

2008

Abstract The reaction of 1-nitronaphthalene ( 1 ) with the Danishefsky diene ( 2 ) to give the dihydrophenanthrene derivative 11 has been theoretically studied using DFT methods. This reaction is a domino process that is initialized by a polar Diels–Alder reaction between 1 and 2 to give the formally [2 + 4] cycloadduct 3 . The subsequent concerted elimination of nitrous acid ( 4 ) from 3 yields 11 . Analysis of the global reactivity indices as well as the thermodynamic data for this domino process indicate that while the large electrophilic character of 1 together with the large nucleophilic character of 2 are responsible for the participation of these reagents in a polar Diels–Alder react…

DieneCondensed Matter PhysicsPhotochemistryBiochemistrychemistry.chemical_compoundElimination reactionNucleophilechemistryCascade reactionComputational chemistryReagentElectrophileReactivity (chemistry)Physical and Theoretical ChemistryDerivative (chemistry)Journal of Molecular Structure: THEOCHEM
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Theoretical study on the mechanism of the domino reactions of tertiary α-cyano-enamines and dimethyl acetylenedicarboxylate

2001

Abstract The mechanisms of the domino reaction between dimethyl acetylenedicarboxylate, 1 , and 2-( N , N -dimethylamino)acrylonitrile, 2 , and these in presence of acrylonitrile have been theoretically studied using ab initio methods. These domino reactions comprise several pericyclic-type reactions. The geometrical and electronic analysis of the HF/6-31G ∗ transition structures and intermediates allows characterizing the processes that take place along these domino reactions. B3LYP/6-31G ∗ energetic results are in agreement with the experimental outcomes.

Dimethyl acetylenedicarboxylatechemistry.chemical_compoundPericyclic reactionchemistryCascade reactionComputational chemistryOrganic ChemistryDrug DiscoveryAb initioAcrylonitrileBiochemistryDominoTetrahedron
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Understanding the domino reaction between 1-diazopropan-2-one and 1,1-dinitroethylene. A molecular electron density theory study of the [3 + 2] cyclo…

2017

The reaction between 1-diazopropan-2-one and 1,1-dinitroethylene has been studied using the Molecular Electron Density Theory (MEDT) at the B3LYP/6-31G(d,p) computational level. This reaction comprises two domino processes initialised by a common [3 + 2] cycloaddition (32CA) reaction yielding a 1-pyrazoline, which participates in two competitive reaction channels. Along channel I, 1-pyrazoline firstly tautomerises to a 2-pyrazoline, which by a proton abstraction and spontaneous loss of nitrite anion yields the final pyrazole, while along channel II, the thermal extrusion of the nitrogen molecule in 1-pyrazoline gives a very reactive diradical intermediate which quickly yields the final gem-…

Electron density010405 organic chemistryDiradicalGeneral Chemical EngineeringGeneral ChemistryPyrazole010402 general chemistryPhotochemistry01 natural sciencesDominoCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionElectrophileReactivity (chemistry)RSC Advances
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A combined experimental and theoretical study of the thermal [3+2] cycloaddition of carbonyl ylides with activated alkenes

2018

International audience; 4-Benzoyl-3,5-diaryltetrahydrofuran-2,2-dicarbonitriles were first synthesized from 2,2-dicyano-3-aryloxiranes and chalcones at toluene reflux; the 4,5-cis products proved to be predominantly formed and were isolated. Whereas shortened reaction times were observed by using microwave irradiation or catalytic cuprous chloride, no significant stereoselectivity change was in general noticed. Reacting 2,2-dicyano-3-aryloxiranes with 2-cyclopentenone next afforded 3-aryl-4-oxohexahydro-1H-cyclopenta[c]furan-1,1-dicarbonitriles, and the endo stereoisomers were isolated. That no stereoselectivity change was noticed in the presence of cuprous chloride rather suggests an impac…

Epoxide010402 general chemistryenones01 natural sciencesMedicinal chemistryAnalytical ChemistryCatalysisInorganic Chemistrychemistry.chemical_compound[SDV.SP.MED]Life Sciences [q-bio]/Pharmaceutical sciences/MedicationCascade reaction[3+2] cycloadditionEnamines[CHIM]Chemical SciencesTetrahydrofuransSpectroscopytheoretical calculationschemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryRegioselectivityCycloaddition0104 chemical sciencescarbonyl ylideschemistryYlide[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyStereoselectivityCis–trans isomerismJournal of Molecular Structure
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Understanding the domino reaction between 3-chloroindoles and methyl coumalate yielding carbazoles. A DFT study.

2014

The molecular mechanism of the reaction between N-methyl-3-chloroindole and methyl coumalate yielding carbazole has been studied using DFT methods at the MPWB1K/6-311G(d,p) level in toluene. This reaction is a domino process that comprises three consecutive reactions: (i) a polar Diels-Alder (P-DA) reaction between indole and methyl coumalate yielding two stereoisomeric [2 + 4] cycloadducts (CAs); (ii) the elimination of HCl from these CAs affording two stereoisomeric intermediates; and (iii) the extrusion of CO2 in these intermediates, finally yielding the carbazole. This P-DA reaction proceeds in a completely regioselective and slightly exo selective fashion. In spite of the highly polar …

Exergonic reactionIndole testCarbazoleOrganic ChemistryRegioselectivityPhotochemistryBiochemistrychemistry.chemical_compoundElimination reactionCascade reactionchemistryComputational chemistryReagentReactivity (chemistry)Physical and Theoretical ChemistryOrganicbiomolecular chemistry
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PERFORMANCE EVALUATION OF CASCADE REFRIGERATION SYSTEMS USING DIFFERENT REFRIGERANTS

2012

Due to the negative effects of synthetic refrigerants on the environment, natural refrigerants have obtained again interest as alternative refrigerants for different applications because of their zero ODP and negligible GWP. This paper presents a thermodynamic analysis of different two-stage cascade refrigeration systems using as refrigerant carbon dioxide (R744) in low-temperature circuit, and, respectively, ammonia (R717), propane (R290), butane (R600), R404A, R410A and R134a in high-temperature circuit. The operating parameters considered in this study include condensing and evaporating temperatures in high-temperature circuit, temperature difference in the cascade heat exchanger, and e…

Fluid Flow and Transfer ProcessesMaterials scienceCascade refrigerationRenewable Energy Sustainability and the EnvironmentThermodynamicsButaneRefrigerantchemistry.chemical_compoundchemistryControl and Systems EngineeringCascadePropaneHeat exchangerSettore ING-IND/10 - Fisica Tecnica IndustrialeCascade refrigeration system thermodynamic analysis natural refrigerantsTemperature difference
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Dual Hydrogen Bond - Enamine Catalysis Enables a Direct Enantioselective Three-Component Domino Reaction

2011

A dual system, composed of an enantioselective enamine catalyst and a multiple-hydrogen-bond catalyst achieves the three-component enantioselective aldehyde—nitroalkene—aldehyde domino reaction using either two similar or two different aldehydes.

Hydrogen bond catalysisComponent (thermodynamics)Hydrogen bondChemistryEnantioselective synthesisGeneral MedicineGeneral ChemistryCatalysisCatalysisEnaminechemistry.chemical_compoundCascade reactionOrganocatalysisOrganic chemistryta116Angewandte Chemie Intermational Edition
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