Search results for "Pyrrole"

showing 10 items of 311 documents

Enantioselective Zirconium-Catalyzed Friedel−Crafts Alkylation of Pyrrole with Trifluoromethyl Ketones

2009

The first catalytic enantioselective Friedel-Crafts alkylation of pyrrole with 2,2,2-trifluoroacetophenones to give pyrroles with a trifluoromethyl-substituted tertiary alcohol moiety bearing a quaternary stereogenic center is described. The reaction is achieved in the presence of a 3,3'-dibromo-BINOL-Zr(IV) complex to give the expected products with high yields (up to 98%) and good enantioselectivities (up to 93% ee). The absolute stereochemistry of the products has been determined by chemical correlation.

TrifluoromethylAlkylationOrganic ChemistryEnantioselective synthesisStereoisomerismKetonesAlkylationBiochemistryMedicinal chemistryCatalysisSubstrate SpecificityCatalysisStereocenterchemistry.chemical_compoundchemistryMoietyPyrrolesZirconiumPhysical and Theoretical ChemistryFriedel–Crafts reactionPyrroleOrganic Letters
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Synthesis of 5H-pyrido[3,2-b]pyrrolizin-5-one tripentone analogs with antitumor activity

2018

Abstract Pyrrolizinones represent an interesting class of compounds with varied degrees of structural complexity and pharmacological activity. Among these, 9H-pyrido[2,3-b]pyrrolizin-9-one, tripentone analogs, recently reported by us, showed significant antiproliferative activity against human tumor cell lines, inducing apoptosis and not affecting viability of Caco-2 differentiated in normal intestinal-like cells. Considering their interesting biological activity, their 5H-pyrido[3,2-b]pyrrolizin-5-one analogs were efficiently synthesized in good to excellent yields (61–91%). All tripentone derivatives were tested to assess their cytotoxicity against two human tumor cell lines, HCT-116 (hum…

TripentonesPyridinesAntineoplastic AgentsApoptosisAntiproliferative activity5H-pyrido[3; 2-b]pyrrolizin-5-ones; Antiproliferative activity; Antitumor; Apoptosis; Tripentones; Pharmacology; Drug Discovery3003 Pharmaceutical Science; Organic Chemistry010402 general chemistry01 natural sciencesStructure-Activity Relationship2-b]pyrrolizin-5-onesCell Line TumorNeoplasmsDrug DiscoverymedicineHumansCytotoxic T cellPyrrolesCytotoxicityMitosisIC505H-pyrido[32-b]pyrrolizin-5-onePharmacology010405 organic chemistryChemistryDrug Discovery3003 Pharmaceutical ScienceOrganic Chemistry5H-pyrido[3ApoptosiTripentoneCancerBiological activityAntitumorGeneral MedicineHCT116 Cellsmedicine.disease0104 chemical sciencesCell cultureApoptosisMCF-7 CellsCancer researchCaco-2 CellsDrug Screening Assays AntitumorEuropean Journal of Medicinal Chemistry
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A Short Synthesis of Polysubstituted Pyrrolidines via α-(Alkylidene­amino)nitriles

2004

α-(Alkylideneamino)nitriles can be deprotonated under mild conditions. Their conjugated anions react with enones in a 1,4-addition to yield δ-keto-α-(alkylideneamino)nitriles which in turn can be reduced to form pyrrolidines in a one-pot reaction sequence.

Turn (biochemistry)DeprotonationReaction sequenceChemistryYield (chemistry)Organic ChemistryOrganic chemistryAmino nitrilesGeneral MedicineConjugated systemMedicinal chemistryPyrrole derivativesSynlett
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New Fluorinated 1,3-Vinylogous Amidines as Versatile Intermediates: Synthesis of Fluorinated Pyrimidin-2(1H)-ones.

2006

The condensation of the azaenolates derived from readily available ketimines with fluorinated nitriles offers an efficient and straightforward entry to new fluorinated 1,3-vinylogous amidines. These versatile compounds, in turn, react with triphosgene to yield new fluorinated pyrimidin-2(1H)-ones in high yields.

Turn (biochemistry)chemistry.chemical_compoundTriphosgeneChemistryYield (chemistry)Organic ChemistryDrug DiscoveryCondensationOrganic chemistryGeneral MedicineBiochemistryPyrrole derivativesChemInform
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Theoretical characterization of the lowest-energy absorption band of pyrrole

2002

The lowest-energy band of the electronic spectrum of pyrrole has been studied with vibrational resolution by using multiconfigurational second-order perturbation theory (CASPT2) and its multistate extension (MS–CASPT2) in conjunction with large atomic natural orbital-type basis sets including Rydberg functions. The obtained results provide a consistent picture of the recorded spectrum in the energy region 5.5–6.5 eV and confirm that the bulk of the intensity of the band arises from a ππ∗ intravalence transition, in contradiction to recent theoretical claims. Computed band origins for the 3s,3p Rydberg electronic transitions are in agreement with the available experimental data, although new…

Valence (chemistry)Organic compounds ; Vibrational states ; Perturbation theory ; Rydberg states ; Orbital calculationsAb initioGeneral Physics and AstronomyPerturbation theoryRydberg statesUNESCO::FÍSICA::Química físicaOrbital calculationschemistry.chemical_compoundsymbols.namesakechemistryEnergy absorptionAtomic electron transitionExcited stateOrganic compoundsRydberg formulasymbolsTheoretical chemistryVibrational statesPhysical and Theoretical ChemistryAtomic physics:FÍSICA::Química física [UNESCO]Pyrrole
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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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Highly Enantioselective Friedel−Crafts Alkylations of Indoles with Simple Enones Catalyzed by Zirconium(IV)−BINOL Complexes

2007

Complexes of BINOL-based ligands with Zr(OtBu)4 catalyze the Friedel-Crafts alkylation reaction of indoles and pyrrole with nonchelating beta-substituted alpha,beta-enones at room temperature affording the expected products with good yields and ee above 95% in most of the studied examples.

ZirconiumOrganic ChemistryEnantioselective synthesischemistry.chemical_elementGeneral MedicineAlkylationBiochemistryPyrrole derivativesCatalysischemistry.chemical_compoundchemistrySimple (abstract algebra)Organic chemistryPhysical and Theoretical ChemistryFriedel–Crafts reactionPyrroleOrganic Letters
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ChemInform Abstract: Enantioselective Synthesis of Tertiary Alcohols Through a Zirconium-Catalyzed Friedel-Crafts Alkylation of Pyrroles with α-Ketoe…

2011

Chiral complexes of 1,1′-bi-2-naphthol-based ligands with zirconium tert-butoxide catalyze the Friedel–Crafts alkylation of pyrroles with α-ketoesters to afford tertiary alcohols in good yields and ee up to 98%. The reaction is also of application to 4,7-dihydroindole to give C2-alkylated indoles after oxidation with p-benzoquinone.

ZirconiumchemistryEnantioselective synthesischemistry.chemical_elementOrganic chemistryGeneral MedicineAlkylationFriedel–Crafts reactionTertiary alcoholsPyrrole derivativesCatalysisChemInform
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ChemInform Abstract: Synthesis of Functionalized Indoles with a Trifluoromethyl-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselect…

2010

Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

Zirconiumchemistry.chemical_compoundCarbon atomTrifluoromethylchemistryEnantioselective synthesischemistry.chemical_elementGeneral MedicineAlkylationMedicinal chemistryFriedel–Crafts reactionPyrrole derivativesStereocenterChemInform
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The role of side chains in Substituted Pyrrole derivatives towards antiproliferative activity

2014

In the last years, the introduction of side chains in different molecular compounds takes increasing importance. As recently reported in literature, heterocyclic scaffolds with poor biological activity , if properly decorated with selected side chains, can improve their anticancer activity against a large spectrum of human tumor cell lines. For example, the annelated Pyrrolo[3,4-e]Pyrimidines and Pyrrolo[3,2-e]Pyrimidines, opportunely functionalized with a large number of side chains, showed a good increase in the antitumor activity with respect to the starting core structure. New compound thus obtained showed antiproliferative activity against all the human tumor cells, generally in the lo…

antiproliferative activityPyrrole derivativeSettore CHIM/08 - Chimica Farmaceutica
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