Search results for " Bases"

showing 10 items of 272 documents

Efficient Addition of Acid Enediolates to Epoxides

2004

We report new conditions to facilitate the addition of dianions of carboxylic acids to epoxides as an alternative method to the use of aluminum enolates. These conditions require the use of a sub-stoichiometric (10%) amount of amine for dianion generation and the previous activation of the epoxide with LiCl. Other Lewis acids have been shown to be less effective. Yields are good but only low diastereoselectivity is attained, which has not been controlled despite attempts at optimization. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

Alternative methodschemistry.chemical_compoundNucleophilic additionchemistryOrganic ChemistryEpoxideLithium chlorideRegioselectivityOrganic chemistryAmine gas treatingLewis acids and basesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Low-loading asymmetric organocatalysis

2011

Asymmetric organocatalysis is now recognized as the third pillar of asymmetric synthesis. Recent years have witnessed increasing interest towards the use of highly active and stereoselective organocatalysts. This critical review documents the advances in the development of chiral organocatalysts which are systematically used in ≤3 mol% loading in all the sub-areas of the field, namely aminocatalysis, Brønsted acids and bases, Lewis acids and bases, hydrogen bond-mediated catalysis, phase transfer and N-heterocyclic carbene catalyses (194 references).

AminocatalysisMolecular StructureOrganic chemicalsBronsted BaseEnantioselective synthesisPillarSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCatalysisBronsted acidCatalysisoragnocatalysichemistry.chemical_compoundchemistryphase-transfer catalysiOrganocatalysisOrganic chemistryLewis acids and basesOrganic ChemicalsBrønsted–Lowry acid–base theoryCarbeneChem. Soc. Rev.
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The Crucial Role of Polyatomic Anions in Molecular Architecture: Structural And Magnetic Versatility of Five Nickel(II) Complexes Derived from A N,N,…

2009

Five new nickel(II) complexes [Ni(2)L(2)(N(3))(2)(H(2)O)(2)] (1), [Ni(2)L(2)(NO(3))(2)] (2), [Ni(2)L(2)(O(2)CPh)(CH(3)OH)(2)]ClO(4).0.5CH(3)OH (3), [Ni(3)L(2)(O(2)CPh)(4)] (4), and [Ni(2)L(2)(NO(2))(2)](n) (5) have been synthesized by using a tridentate Schiff base ligand, HL (2-[(3-Methylamino-propylimino)-methyl]-phenol), and the polyatomic monoanions N(3)(-), NO(3)(-), PhCOO(-), or NO(2)(-). The complexes have been structurally and magnetically characterized. The structural analysis reveals that in all five complexes, the Ni(II) ions possess a distorted octahedral geometry. Complexes 1 and 2 are dinuclear with di-mu-1,1-azido and di-mu(2)-phenoxo bridges, respectively. Complex 3 is also …

AnionsSchiff baseMolecular StructureSpectrophotometry InfraredLigandStereochemistryPolyatomic ionchemistry.chemical_elementCrystallography X-RayLigandsIonInorganic ChemistryMagneticschemistry.chemical_compoundNickelCrystallographychemistryNickelOctahedral molecular geometryCarboxylatePhysical and Theoretical ChemistrySchiff BasesInorganic Chemistry
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Understanding the cooperative NHC/LA catalysis for stereoselective annulation reactions with homoenolates. A DFT study.

2011

The role of Ti(Oi-Pr)(4) Lewis acid (LA) in the cooperative N-heterocyclic carbene (NHC)/LA catalyzed addition of enals to enones to yield cis-cyclopentenes has been investigated using DFT methods at the B3LYP/6-31G** computational level. Ti(IV) effectively catalyzes the reaction by formation of a complex with cinnamaldehyde 1, which favors the nucleophilic attack of NHC 5 on 1, and the subsequent proton abstraction to yield the extended Ti(IV)-Breslow intermediate 21. The nature of the metal involved in the LA catalyst plays a relevant role due to the more basic character of NHCs than aldehydes. Thus, strong LAs, such as Zn(OTf)(2), prevent the catalytic behavior of NHCs to form a very sta…

AnnulationStereochemistryOrganic ChemistryBiochemistryCatalysischemistry.chemical_compoundchemistryNucleophileYield (chemistry)StereoselectivityLewis acids and basesPhysical and Theoretical ChemistryCarbeneCis–trans isomerismOrganicbiomolecular chemistry
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Oxidative transformation of aryls using molybdenum pentachloride.

2012

Molybdenum pentachloride combines a strong Lewis acid character with an unusually high oxidation potential creating a powerful reagent for oxidative transformations. Since the oxidative coupling reaction of aryls is induced at an extraordinarily high reaction rate, a variety of labile groups, e.g. iodo, tert-alkyl, etc., are tolerated on the aromatic core. Furthermore, the co-formed molybdenum salts can either be exploited for template effects to obtain uncommon geometries in a preferred manner, or redox-play starts after aqueous workup. Therefore MoCl(5) represents a unique and easily available reagent.

Aqueous solutionMetals and Alloyschemistry.chemical_elementGeneral ChemistryOxidative phosphorylationMolybdenum pentachlorideCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReaction ratechemistryMolybdenumReagentMaterials ChemistryCeramics and CompositesOrganic chemistryOxidative coupling of methaneLewis acids and bases
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DFT computational study on Fe(III)-N,N′-ethylene-bis(salicylideneiminato) derivatives

2005

DFT calculations, at unrestricted B3LYP level, have been performed on the structures of three iron(III) complexes, Fe(Salen)Cl, [Fe(Salen)]+ and [Fe(Salen)OH2]+, where Salen is the anion of Schiff base ligand N,N′-ethylene-bis (salicylideneimine), considering the spin multiplicity (S) values 2, 4 and 6. The results obtained have been compared with the available structural an magnetic experimental data, allowing us to conclude that a stable form of the FeIII(Salen) complex in aqueous solution should be characterized by an energy stabilization of the S=4 compared to the S=6 state.

Aqueous solutionSchiff baseLigandInorganic chemistryCondensed Matter PhysicsBiochemistryIonEthylene bisCrystallographychemistry.chemical_compoundchemistryMetal salen complexesPhysical and Theoretical ChemistryIron Schiff bases Salen Density functional calculationsSettore CHIM/02 - Chimica Fisica
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Glycosyl azides as building blocks in convergent syntheses of oligomeric lactosamine and Lewisx saccharides

1997

Abstract Oligosaccharides containing type 2 lactosamine repeating units, e.g. neo-lacto-octaose and trimeric Lewis x derivatives, are constructed using neo-lactosamine azide building blocks. The azido group provides a favorable protection of the anomeric position which is stable to versatile protecting group manipulations and glycosylation reactions. On the other hand, glycosyl azides can be converted into glycosyl fluorides via a 1,3-dipolar cycloaddition with di- tert -butyl-acetylenedicar☐ylate and subsequent treatment of the resulting N -glycosyl triazoles with hydrogen fluoride-pyridine complex. Activation of the lactosamine fluorides with Lewis acids affords the possibility to extend …

AzidesMagnetic Resonance SpectroscopyGlycosylationChemistryStereochemistryMolecular Sequence DataOrganic ChemistryClinical BiochemistryChemical glycosylationDisaccharideLewis X AntigenPharmaceutical ScienceAmino SugarsBiochemistrychemistry.chemical_compoundCarbohydrate SequenceDrug DiscoveryCarbohydrate ConformationMolecular MedicineGlycosylLewis acids and basesAzideGlycosyl donorProtecting groupMolecular BiologyBioorganic & Medicinal Chemistry
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o-(Hydroxyalkyl)phenyl P-Chirogenic Phosphines as Functional Chiral Lewis Bases

2013

The stereoselective synthesis of P-chirogenic phosphines bearing an o-hydroxyalkyl chelating arm is described. The synthesis is based either on the hydroxyalkylation of P-chirogenic o-bromophenylphosphines (borane) or on their carbonatation and then reduction. The hydroxyalkylation with benzaldehyde or pivalaldehyde affords a mixture of epimers which are isolated by chromatography and characterized by their X-ray structures. Preliminary assays of free P-chirogenic o-(hydroxyalkyl)phenyl phosphines, as new functional Lewis bases in catalyzed asymmetric aza-MBH reaction, lead to β-aminoester derivatives with ee values up to 74%.

Benzaldehydechemistry.chemical_compoundStereochemistryChemistryOrganic ChemistryEpimerStereoselectivityChelationLewis acids and basesPhysical and Theoretical ChemistryBoraneBiochemistryCatalysisOrganic Letters
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Promoting Deoxygenation of Bio-Oil by Metal-Loaded Hierarchical ZSM-5 Zeolites

2016

3 Figuras.- 5 tablas.-1 Esquema.- This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Sustainable Chemistry & Engineering, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acssuschemeng.5b01606 ”

Bio-oil upgradingGeneral Chemical EngineeringInorganic chemistryLignocellulosic biomass02 engineering and technology01 natural sciencesCatalysisEnvironmental ChemistryOrganic chemistryLewis acids and basesZeoliteMetal loadingDeoxygenationIon exchange010405 organic chemistryRenewable Energy Sustainability and the EnvironmentChemistryDecarbonylationDeoxygenationGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesZSM-50210 nano-technologyHierarchical ZSM-5 zeoliteACS Sustainable Chemistry & Engineering
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Interesterification of rapeseed oil catalyzed by tin octoate

2014

The interesterification of rapeseed oil was performed for the first time by using tin octoate as Lewis acid homogeneous catalysts and methyl or ethyl acetate as acyl acceptors in a batch reactor, within the temperature range 393–483 K. The yields in fatty acid ethyl esters (FAEE) and triacetin (TA) after 20 h of reaction time increased from 8% and 2%–to 61% and 22%, respectively, when the reaction temperature increased from 423 to 483 K. An optimum value of 40 for the acyl acceptor to oil molar ratio was found to be necessary to match good fatty acid alkyl ester yields with high enough reaction rate. The rate of generation of esters was significantly higher when methyl acetate was used as a…

BiodieselRenewable Energy Sustainability and the EnvironmentInteresterified fatMethyl acetateEthyl acetateForestryCatalysisReaction ratechemistry.chemical_compoundchemistryOrganic chemistryLewis acids and basesWaste Management and DisposalAgronomy and Crop ScienceTriacetinBiomass and Bioenergy
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