Search results for "Bases"

showing 10 items of 1240 documents

Synthesis of Functionalized Indoles with an α-Stereogenic Ketone Moiety Through an Enantioselective Friedel-Crafts Alkylation with (E)-1,4-Diaryl-2-b…

2009

Chiral complexes of BINOL-based ligands with hafnium tert-butoxide catalyze the enantioselective Friedel-Crafts alkylation of indoles with (E)-1,4-diaryl-2-butene-1,4-diones at room temperature, with good yields and ee up to 94%. Hafnium(IV) was found to be a more effective Lewis acid than other frequently used metal ions such as titanium(IV) or zirconium(IV). Unlike the enantioselective Friedel-Crafts alkylation of indoles with α,β-unsaturated compounds where the stereogenic center is generated in the β-position to a carbonyl group, the Friedel-Crafts alkylation with 2-butene-1,4-diones described here generates an α-stereogenic center with respect to one of the carbonyl groups. This can be…

chemistry.chemical_classificationKetonechemistryEnantioselective synthesisMoietyOrganic chemistryGeneral ChemistryLewis acids and basesAlkylationFriedel–Crafts reactionMedicinal chemistryStereocenterUmpolungAdvanced Synthesis & Catalysis
researchProduct

Linked Benzylamido-Cyclopentadienyl Ligands: Synthesis and Characterization of Alkyl Titanium Complexes

1997

Titanium complexes of the general type Ti(η5:η1-C5H4Si-Me2NCH2C6H3X2-2,5)Cl2 (XH, F), containing a linked benzylamido-cyclopentadienyl ligand, were prepared by reaction of Ti(η5-C5H4SiMe2Cl)Cl3 with lithium amide Li(NHCH2C6H3X2-2,5). A single-crystal X-ray structural analysis of Ti(η5: η1-C5H4SiME2NCH2C6H3F2-2,5)Cl2 revealed a conformation in the solid state in which the aryl ring is turned away from the metal center. Ti(η5:η1-C5H4SiMe2NCH2C6H5)Cl2 can be alkylated with a variety of reagents to form extremely sensitive complexes of the type Ti(η5-C5H4SiMe,2NCH2C6H5)R2 (RMe, CH2 C6H5, CH2SiME3, CH2CMe2C6H5). Reaction of Li2[C5Me4SiMe2NCH2C6H5] with TiCl3(THF)3 gave Ti(η5: η1-C5Me4SiMe2NCH2C6…

chemistry.chemical_classificationLithium amideLigandStereochemistryArylchemistry.chemical_elementAlkylationInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCyclopentadienyl complexLewis acids and basesAlkylTitaniumChemische Berichte
researchProduct

Block and graft copolymers of 2-oxazolines

1994

The cationic ring-opening polymerization of 2-oxazolines is known to be initiated by alkyl halides, Lewis acids and esters of strong acids. The polymerization proceeds by a living mechanism. Numerous block and graft copolymers have already been described. Recently it was found that chloroformates (R-O-CO-CI) are also useful initiators. The mechanism of the initiation and propagation is discussed. This type of initiators allows the synthesis of different novel two-block and three-block copolymers, star-shape polymers, and a graft copolymer with a polyvinylacetate backbone.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStrong acidsOrganic ChemistryCationic polymerizationPolymerCondensed Matter PhysicsBlock (periodic table)chemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerLewis acids and basesAlkylMacromolecular Symposia
researchProduct

Structure-based statistical analysis of transmembrane helices

2012

Recent advances in determination of the high-resolution structure of membrane proteins now enable analysis of the main features of amino acids in transmembrane (TM) segments in comparison with amino acids in water-soluble helices. In this work, we conducted a large-scale analysis of the prevalent locations of amino acids by using a data set of 170 structures of integral membrane proteins obtained from the MPtopo database and 930 structures of water-soluble helical proteins obtained from the protein data bank. Large hydrophobic amino acids (Leu, Val, Ile, and Phe) plus Gly were clearly prevalent in TM helices whereas polar amino acids (Glu, Lys, Asp, Arg, and Gln) were less frequent in this …

chemistry.chemical_classificationModels MolecularChemistryCell MembraneBiophysicsComputational BiologyMembrane ProteinsWaterHelix-turn-helixGeneral MedicineBiofísicaProtein Structure SecondaryAmino acidTransmembrane domainCrystallographyMembrane proteinSolubilitySeqüència d'aminoàcidsHelixChou–Fasman methodThermodynamicsDatabases ProteinIntegral membrane proteinHydrophobicity scales
researchProduct

(Co-)solvent selection for single-wall carbon nanotubes: best solvents, acids, superacids and guest-host inclusion complexes.

2011

Analysis of 1-octanol-water, cyclohexane-water and chloroform (CHCl(3))-water partition coefficients P(o-ch-cf) allows calculation of molecular lipophilicity patterns, which show that for a given atom log P(o-ch-cf) is sensitive to the presence of functional groups. Program CDHI does not properly differentiate between non-equivalent atoms. The most abundant single-wall carbon nanotube (SWNT), (10,10), presents a relatively small aqueous solubility and large elementary polarizability, P(o-ch-cf) and kinetic stability. The SWNT solubility is studied in various solvents, finding a class of non-hydrogen-bonding Lewis bases with good solubility. Solvents group into three classes. The SWNTs in so…

chemistry.chemical_classificationModels MolecularCyclodextrinChemistryNanotubes CarbonAmylopectinCationic polymerizationStarchSolventPartition coefficientColloidGlucoseSolubilityLipophilicityLewis BasesSolventsPhysical chemistryOrganic chemistryNanotechnologyThermodynamicsGeneral Materials ScienceLewis acids and basesSolubilityAcidsNanoscale
researchProduct

The role of Zn2+ in enhancing the rate and stereoselectivity of the aldol reactions catalyzed by the simple prolinamide model

2011

Abstract The aldol reaction between acetone and 4-nitrobenzaldehyde catalyzed by single l -prolinamide and its zinc complexes has been studied. An increase in the rate and the stereoselectivity of the reaction has been shown by using zinc derivatives. A mechanistic proposal, based on NMR and ESI studies, has been put forward to explain the experimental data: zinc–prolinamide complexes catalyze the reaction following the general mechanism of stereoselective enamine nucleophilic addition to the acceptor aldehyde. Zn2+ prevents the nonspecific base-catalyzed reaction by diminishing the basicity of the amine nitrogen of prolinamide.

chemistry.chemical_classificationNucleophilic additionOrganic ChemistryBiochemistryAldehydeCombinatorial chemistryCatalysisEnaminechemistry.chemical_compoundchemistryAldol reactionDrug DiscoveryOrganic chemistryStereoselectivityAmine gas treatingLewis acids and basesTetrahedron
researchProduct

A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
researchProduct

Carbohydrates as chiral templates: asymmetric ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matrices

1988

Abstract In the presence of Lewis acid catalysts O-acetyl- (1) and O-pivaloyl- (2) protected β-D-galactopyranosylamines react with aldehydes, isocyanides and carboxylic acids in Ugi-four-component-condensations to give the corresponding N-galactosyl-amino acid amide derivatives 3,5 in almost quantitative yields. Zinc chloride is the most effective Lewis acid catalyst. At 0°C or even at room temperature the (2R,β-D)-diastereomers of the amino acid derivatives 3,5 are formed with high diastereoselectivity. If the sterically more demanding O-pivaloyl galactosylamine 2 is used at -78°C to -25°C the stereoselectivity often exeeds 20:1 favouring the (2R,β-D) diastereomers 5. After one recrystalli…

chemistry.chemical_classificationOrganic ChemistryDiastereomerBiochemistryAmino acidCatalysisLewis acid catalysischemistry.chemical_compoundchemistryAmideDrug DiscoveryOrganic chemistryStereoselectivityAcid hydrolysisLewis acids and basesTetrahedron
researchProduct

Molecular “Floppyness” and the Lewis Acidity of Silanes: A Density Functional Theory Study

2001

A comprehensive set of Lewis acid-base adducts of silanes was investigated by means of the density functional theory geometry optimization [B3LYP/6−31G(d)], and thermochemical calculations, [B3LYP/6−311+G(2d,p)//B3LYP/6−31G(d)]. Complex formation was found to weaken Si−Cl and Si−Br bonds more than Si−F or Si−H bonds. Comparable distances between Si and a Lewis base L (L = NH3, OH2, F−) are shorter in hexa- than in pentacoordinated complexes. The molecular structures of the pentacoordinated Si complexes allowed for a mapping of an SN2 reaction pathway by correlating the lengths of the Si−X and Si−L bonds. Complex formation was found to be exothermic for most of the coordination compounds, an…

chemistry.chemical_classificationSilanesStereochemistryEnthalpyIonic bondingCoordination complexAdductInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryDonor numberThermochemistryLewis acids and basesEuropean Journal of Inorganic Chemistry
researchProduct

Mesoporous Materials Incorporating Metal Triflates

2016

Metal triflates attracted a large interest as catalysts in the past three decades especially due to the Lewis acid properties exhibited by these compounds and the variety of the functional group transformations. This chapter proposes an overview presenting the catalytic performances of triflates both as molecular compounds and as triflates dispersed in different solid matrices. In the first part the performances of molecular triflates in organic reactions carried out in the presence of water or water as solvent considering both water-sensitive and -insensitive metals are discussed. Then, the importance of materials incorporating triflates is demonstrated for catalysts obtained via immobiliz…

chemistry.chemical_classificationSolventchemistry.chemical_compoundOrganic reactionChemistryFunctional groupOrganic chemistryPolymerLewis acids and basesMesoporous materialCombinatorial chemistryCatalysisCharacterization (materials science)
researchProduct