Search results for "Isoindole"

showing 10 items of 83 documents

Electronic structure of metal‐free phthalocyanine : A valence effective Hamiltonian theoretical study

1988

We present a valence effective Hamiltonian (VEH) nonempirical investigation of the electronic properties of metal‐free phthalocyanine. The valence one‐electron energy levels are related to those of the phthalocyanine components: benzene, pyrrole, and isoindole. From the electronic structure standpoint, phthalocyanine has to be viewed as formed by joining four benzene moieties to the central carbon–nitrogen ring rather than by combining four isoindole units through nitrogen bridges. Comparison of the VEH density‐of‐valence‐states curves with the experimental ultraviolet photoelectron spectroscopy (UPS) data is quantitatively excellent and allows for a complete interpretation of the experimen…

Valence (chemistry)PhthalocyaninesPhotoelectron SpectroscopyGeneral Physics and AstronomyElectronic structurePhthalocyanines ; Electronic Structure ; Valence ; Hamiltonian Function ; Photoelectron SpectroscopyPhotochemistryUNESCO::FÍSICA::Química físicachemistry.chemical_compoundsymbols.namesakeValenceX-ray photoelectron spectroscopychemistryElectronic StructurePhthalocyaninesymbolsHamiltonian FunctionPhysical chemistryPhysical and Theoretical ChemistryIsoindoleHamiltonian (quantum mechanics):FÍSICA::Química física [UNESCO]Ultraviolet photoelectron spectroscopyPyrrole
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Micellar liquid chromatographic separation of amino acids using pre- and post-column o -phthalaldehyde/ N -acetylcysteine derivatization

2000

Abstract The isocratic analysis of primary proteic amino acids using a C18 column, micellar mobile phases of sodium dodecyl sulphate (SDS) and 1-propanol at varying pH, and pre- and post-column formation of the o-phthalaldehyde (OPA)/N-acetyl- l -cysteine (NAC) isoindoles, is examined. An interpretive optimization strategy was applied to find the best separation conditions. For this purpose, empirical polynomial models were used to describe the elution behavior of the isoindoles and free amino acids, using as separation factors the concentrations of surfactant and modifier (two-factor problem), or these two factors and the pH of the mobile phase (three-factor problem). The separation of the…

chemistry.chemical_classificationAlanineChromatographyIsoindolesPhenylalanineBiochemistryAnalytical ChemistryAmino acidGlutaminechemistryAspartic acidEnvironmental ChemistryThreonineSpectroscopyCysteineAnalytica Chimica Acta
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Retro-Diels-Alder Protocol for the Synthesis of Pyrrolo[1,2-a]pyrimidine and Pyrimido[2,1-a]isoindole Enantiomers

2013

A simple protocol was introduced to prepare several enantiomerically pure heterocycles by using (–)-(1R,2R,3S,4S)-3-aminonorbornene-2-carboxylic acid as a chiral auxiliary. The protocol is based on a domino ring-closure reaction, in which the relative configuration of the new asymmetric center is controlled by the stereochemistry of the amino acid, followed by a microwave-induced retro-Diels–Alder reaction.

chemistry.chemical_classificationChiral auxiliaryPyrimidineStereochemistryOrganic ChemistryDominoAmino acidchemistry.chemical_compoundMicrowave chemistrychemistryDiels alderPhysical and Theoretical ChemistryEnantiomerIsoindoleEuropean Journal of Organic Chemistry
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Chromatographic Determination of Thiols After Pre‐column Derivatization witho‐Phthalaldehyde and Isoleucine

2004

Abstract The reaction of primary amines with excess o‐phthalaldehyde (OPA) and thiol yields unique isoindole derivatives that are readily separated by reversed‐phase liquid chromatography. In a previous work, a spectrophotometric procedure was proposed for the assay of N‐acetylcysteine by derivatization with OPA and isoleucine at pH 9.5, with satisfactory results. The chromatographic determination of this and other low molecular‐weight thiols, after isoindole formation with isoleucine, using mobile phases of acetonitrile–water at pH 3 and spectrophotometric detection, is now examined. From the assayed thiols (thioglycolic acid, 3‐mercaptopropionic acid, tiopronin, N‐acetylcysteine, N‐acetyl…

chemistry.chemical_classificationChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReversed-phase chromatographyBiochemistryAnalytical ChemistryO-Phthalaldehydechemistry.chemical_compoundTioproninmedicineThiolThioglycolic acidIsoleucineDerivatizationIsoindolemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Analysis of amino acids using serially coupled columns.

2017

Single conventional columns in reversed-phase LC are insufficient for analysing the isoindoles of primary amino acids, due to their limited functionality. An interesting possibility for increasing the separation power is the combination of several columns of different nature, where the length is modified by coupling small segments. This approach may require a considerable investment to have multiple lengths for each stationary phase. However, the combination of only two columns of fixed length can be enough to resolve satisfactorily relatively complex mixtures, provided that an optimised gradient program is applied. In this work, a mixture of 19 primary amino acid isoindoles found in protei…

chemistry.chemical_classificationCouplingWork (thermodynamics)Chromatography Reverse-PhaseIndolesIsoindoles010401 analytical chemistryAnalytical chemistryProteinsFiltration and SeparationReversed-phase chromatography010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryAmino acidPrimary amino acidsSolventColumn (typography)chemistryAmino AcidsChromatography High Pressure LiquidJournal of separation science
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Preparation and Structures of Isoindolone- or Pyrimidone-Condensed Heterocycles Containing a Hydroxy Group on a Cyclohexane or Norbornane Moiety

2009

With DL-valinol, 3-amino-1-propanol and o-aminothiophenol, aroyl(bi/tri)cyclic lactones 1 and 2 were cy- clized to isoindole- 4-6, 8, 9, pyrimidinone- 10 or thiazepine- 7 condensed heterocycles. The ketal lactone 3 furnished the benzthiazoloisoindole 9 and mixtures of epimeric hydroxyphthalazinoquinazolinones 11 and 12. The structures were es- tablished by means of 1 H and 13 C NMR spectroscopy and in some cases by X-ray crystallography.

chemistry.chemical_classificationCyclohexaneOrganic ChemistryCarbon-13 NMRBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryThiazepineMoietyPyrimidoneNorbornaneIsoindoleLactoneLetters in Organic Chemistry
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Determination of the protein and free amino acid content in a sample using o-phthalaldehyde and N-acetyl-L-cysteine

1990

A spectrophotometric method is proposed for determining the protein content in a sample after total acid hydrolysis. In the procedure, free amino acids are caused to react with o-phthalaldehyde and N-acetyl-L-cysteine at pH 9.5, using isoleucine as the reference compound. Correction factors are used to take into account the differences between the molar absorptivities of the amino acid isoindoles and the recoveries of the amino acids after the hydrolysis treatment. The limit of detection was in the range 40-50 micrograms of protein, and the recoveries were usually 101 +/- 3% with a coefficient of variation lower than 4%. The free amino acid content in a partially hydrolysed protein was also…

chemistry.chemical_classificationDetection limitChromatographyIsoindolesmedicine.diagnostic_testHydrolysisProteinsBiochemistryXanthoproteic reactionAcetylcysteineAnalytical ChemistryAmino acidHydrolysisO-PhthalaldehydechemistrySpectrophotometrySpectrophotometryElectrochemistrymedicineEnvironmental ChemistryAmino AcidsIsoleucineo-PhthalaldehydeSpectroscopyThe Analyst
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Spectrophotometric determination of cystine by formation of an o-phthalaldehyde/N-acetyl-l-cysteine derivative

1989

Abstract Cystine reacts with o -phthalaldehyde (OPA) in the absence and presence of a thiol compound to yield different compounds. The use of N -acetyl- l -cysteine as thiol leads to the formation of two derivatives, likely simple and double isoindoles, where the disulfide bond remains unbroken. In contrast, mercaptoethanol gives rise to the reduction of the amino acid to form a cysteine derivative. Obtaining cystine isoindoles makes it possible to spectrophotometrically determine the amino acid after Chromatographic separation and is further evidence of the large stabilization effect produced by N -acetyl- l -cysteine in the formation of OPA-thiol derivatives.

chemistry.chemical_classificationIsoindolesStereochemistryCystineMedicinal chemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundO-PhthalaldehydechemistryYield (chemistry)ThiolSpectroscopyPhthalaldehydeCysteineMicrochemical Journal
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Nucleophilic substitutions in the isoindole series as a valuable tool to synthesize derivatives with antitumor activity

2011

Abstract A novel synthetic approach to the synthesis of 3-substituted isoindoles through nucleophilic substitution of 3-halo derivatives by charged carbon, and neutral nitrogen, oxygen, and sulfur nucleophiles, assisted by a 1-acyl group, is reported. Aryl-thio-isoindoles, obtained through a direct nucleophilic substitution with sulfur nucleophiles, showed cytotoxic activity, with GI50 values from micromolar to sub-micromolar concentrations, against the total number of cell lines investigated.

chemistry.chemical_classificationKetoneIsoindolesTertiary amineStereochemistryChemistryIsoindoles Nucleophilic substitutionsColchicine analoguesOrganic ChemistryIsoindoles Nucleophilic substitutions; Antitumor activity; Docking; Colchicine analoguesBiochemistryCombinatorial chemistryChemical synthesisSettore CHIM/08 - Chimica FarmaceuticaDockingchemistry.chemical_compoundIsoindoles Nucleophilic substitutionNucleophileColchicine analogueDrug DiscoveryNucleophilic substitutionAcid hydrolysisIsoindoleAntitumor activity
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Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers

2017

Abstract The synthesis of two enantiomeric pairs of pyrimidoisoindoles 9a, 9b and 10a, 10b is reported. During a domino ring-closure reaction, followed by cycloreversion, the chirality of diendo-(−)-(1R,2S,3R,4S)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxamide [(−)-1] was successfully transfered to heterocycles (+)-9a, (+)-10a, (−)-9b, (−)-10b and (−)-10c.

chemistry.chemical_classificationpharmacyamino acidsheterocycles010405 organic chemistryStereochemistrybiologyOrganic Chemistry010402 general chemistrychemistry01 natural sciencesCatalysis0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundchemistryPhysical and Theoretical ChemistryEnantiomerIsoindoleChirality (chemistry)ta116NorborneneTetrahedron: Asymmetry
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