Search results for "enantioselective synthesis"

showing 10 items of 418 documents

Synthesis, configuration, and calcium modulatory properties of enantiomerically pure 5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylates.

1992

Enantiomerically pure hexahydroquinolinones of the structural type 9 were prepared by a variation of the Hantzsch synthesis in which an optically active acetoacetate served as a chiral auxiliary reagent. Determinations of the de and ee values are described. The absolute configurations of the optically pure products were characterized by single-crystal X-ray analysis. The antipodes 9a and 9b exhibited calcium antagonistic activities on smooth musculature; the (S)-(-)-enantiomer 9b was the more potent compound with regard to the EC50 values which differed by a factor of 100; the intrinsic activity of 9b was 1.2, compared with a value of 0.54 for 9a. On the other hand, R-(+)-9a exerted positiv…

MaleIntrinsic activityGuinea PigsMolecular Conformationchemistry.chemical_elementCalciumQuinolonesMedicinal chemistrychemistry.chemical_compoundX-Ray DiffractionIleumDrug DiscoveryAnimalsHeart AtriaAortaChiral auxiliaryBicyclic moleculeMolecular StructureEnantioselective synthesisAbsolute configurationBiological activityStereoisomerismPapillary MusclesAtrial FunctionCalcium Channel BlockersElectric StimulationchemistryReagentMolecular MedicineFemaleMuscle ContractionJournal of medicinal chemistry
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Enantioselective syntheses of dopaminergic (R)- and (S)-benzyltetrahydroisoquinolines.

2001

Optically pure (1S,R)- and (1R,S)-benzyltetrahydroisoquinolines (BTHIQs), 12a,b as the major diastereomers, were prepared by stereoselective reduction of the isoquinolinium salt possessing (R)- and (S)-phenylglycinol as the chiral auxiliary, respectively. The absolute configurations of (1S,R)-13a hydrochloride (O-debenzoylated derivative from 12a) and (1R,S)-12b diastereomers were unambiguously determined by single-crystal X-ray analysis. Reductive removal of the chiral auxiliary group, subsequent N-propylation, and cleavage of the methylenedioxy group furnished the optically active catecholamines (1S)-16a and (1R)-16b in good overall yield. We have separately prepared for the first time pa…

MaleStereochemistryHydrochlorideDopamineIn Vitro TechniquesCrystallography X-RayLigandsBinding CompetitiveMethylenedioxychemistry.chemical_compoundRadioligand AssayStructure-Activity RelationshipDrug DiscoveryBenzyl CompoundsAnimalsRats WistarChiral auxiliaryChemistryReceptors Dopamine D2Receptors Dopamine D1DopaminergicEnantioselective synthesisDiastereomerStereoisomerismBenzazepinesIsoquinolinesCorpus StriatumRatsRacloprideMolecular MedicineDopamine AntagonistsStereoselectivityEnantiomerSynaptosomes
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Asymmetric Synthesis of Amino-Bis-Pyrazolone Derivatives via an Organocatalytic Mannich Reaction.

2017

A new series of N-Boc ketimines derived from pyrazolin-5-ones have been used as electrophiles in asymmetric Mannich reactions with pyrazolones. The amino-bis-pyrazolone products are obtained in excellent yields and stereoselectivities by employing a very low loading of 1 mol % of a bifunctional squaramide organocatalyst. Depending on the substitution at position 4 of the pyrazolones, the new protocol allows for the generation of one or two tetrasubstituted stereocenters, including a one-pot version combing the Mannich reaction with a base-mediated halogenation. peerReviewed

Mannich reactions010405 organic chemistryChemistryOrganic Chemistryasymmetric synthesisSquaramideEnantioselective synthesisHalogenation010402 general chemistry01 natural sciencespyrazolones0104 chemical sciencesStereocenteramino-bis-pyrazolone productschemistry.chemical_compoundElectrophilePyrazolonesOrganic chemistryBifunctionalMannich reactionta116The Journal of organic chemistry
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Advances in organic and organic-inorganic hybrid polymeric supports for catalytic applications

2016

In this review, the most recent advances (2014–2016) on the synthesis of new polymer-supported catalysts are reported, focusing the attention on the synthetic strategies developed for their preparation. The polymer-supported catalysts examined will be organic-based polymers and organic-inorganic hybrids and will include, among others, polystyrenes, poly-ionic liquids, chiral ionic polymers, dendrimers, carbon nanotubes, as well as silica and halloysite-based catalysts. Selected examples will show the synthesis and application in the field of organocatalysis and metal-based catalysis both for non-asymmetric and asymmetric transformations.

Materials sciencePharmaceutical ScienceAsymmetric catalysiHomogeneous catalysisNanotechnologyReviewCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencesAnalytical ChemistryCatalysislaw.inventionlcsh:QD241-441Heterogeneous catalysiOrganocatalysilcsh:Organic chemistrylawDendrimerDrug DiscoveryOrganic-inorganic hybridOrganic chemistryorganocatalysisPhysical and Theoretical ChemistryPolystyrenechemistry.chemical_classification010405 organic chemistryMedicine (all)Organic ChemistryEnantioselective synthesisasymmetric catalysisPolymerAsymmetric catalysis; Heterogeneous catalysis; Metal catalyst; Organic-inorganic hybrid; Organocatalysis; Polystyrene; Medicine (all); Organic ChemistrySettore CHIM/06 - Chimica OrganicaMetal catalyst0104 chemical sciencesheterogeneous catalysischemistryChemistry (miscellaneous)OrganocatalysisMolecular Medicine
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Asymmetric hydrogenation of ethyl pyruvate over aqueous dispersed Pt nanoparticles stabilized by a cinchonidine-functionalized β-cyclodextrin

2021

International audience; Cinchonidine-functionalized β-cyclodextrin was used as stabilizing agent for platinum nanoparticles dispersed in water, but also as chiral modifier for the asymmetric hydrogenation of ethyl pyruvate at 30 °C under 40 bar of hydrogen. This functionalized cyclodextrin allowed getting more stable, more catalytically active and also more enantioselective Pt nanoparticles compared to control catalytic systems. NMR and MALDI-MS analyses clearly showed the reduction of the vinyl group of the cinchonidine graft during the nanoparticles preparation. Under hydrogen pressure, the hydrogenation of the quinolinic moiety was also proven and can be responsible for the difficul…

Metal nanoparticles010402 general chemistryPlatinum nanoparticles01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundPolymer chemistryCyclodextrinMoiety[CHIM]Chemical SciencesCinchonidineCinchonidinechemistry.chemical_classificationAqueous solutionCyclodextrin010405 organic chemistryChemistryProcess Chemistry and TechnologyAsymmetric hydrogenationEnantioselective synthesisGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisSettore ING-IND/27 - Chimica Industriale E Tecnologica0104 chemical sciencesAsymmetric hydrogenationlcsh:QD1-999Metal nanoparticles Asymmetric hydrogenation Cyclodextrin Cinchonidine
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An enantioselective synthesis of the C(33)–C(37) fragment of Amphotericin B

2003

An enantioselective synthesis of the C(33)–C(37) tripropionate fragment of Amphotericin B has been developed in only 6 steps. Peer reviewed

Models MolecularAntifungal Agentsnatural productsFragment (computer graphics)ChemistryStereochemistryasymmetric synthesisOrganic ChemistryEnantioselective synthesisEstersStereoisomerismLigandsBiochemistryStreptomycesorganic chemistryModels ChemicalAmphotericin BAmphotericin BmedicinePhysical and Theoretical Chemistrymedicine.drugOrg. Biomol. Chem.
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Cooperative Assistance in Bifunctional Organocatalysis: Enantioselective Mannich Reactions with Aliphatic and Aromatic Imines

2012

both of which contain a thiourea moiety (Scheme 1).The catalysts are capable of deprotonating suitable nucleo-philes, such as activated carbonyl compounds. This proton-transfer reaction generates an ion pair, which is composed ofthe protonated catalyst and the anionic nucleophile interact-ing through hydrogen bonds. At least one of the NH moietiesin the protonated catalyst is involved in activating theelectrophilic reaction partner.

Models MolecularHydrogen bond catalysisImineEnantioselective synthesisHydrogen BondingStereoisomerismGeneral MedicineGeneral ChemistryCrystallography X-RayMalonatesCatalysisCatalysischemistry.chemical_compoundchemistryNucleophileOrganocatalysisPolymer chemistryOrganic chemistryMoietyIminesAmino AcidsBifunctionalta116Angewandte Chemie International Edition
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Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and B.

2006

The total synthesis of the proposed structure of feigrisolide A is reported. Ethyl (S)-3-hydroxybutyrate was the chiral starting material. A Brown asymmetric allylation and an Evans aldol reaction were key steps of the synthesis. The NMR data of the synthetic product are different from those of the natural product. The published structure of feigrisolide A is therefore erroneous. A subsequent comparison of spectral data strongly suggests that feigrisolides A and B are identical with (-)-nonactic acid and (+)-homononactic acid, respectively.

Models MolecularMagnetic Resonance SpectroscopyStereochemistryMolecular ConformationStereoisomerismChemical synthesischemistry.chemical_compoundLactonesStructure-Activity RelationshipAldol reactionSpectral dataNatural productMolecular StructureChemistryorganic chemicalsOrganic ChemistryEnantioselective synthesisTotal synthesisStereoisomerismGeneral MedicineNuclear magnetic resonance spectroscopyNmr dataAnti-Bacterial AgentsProduct (mathematics)Aldol condensationStereoselectivityThe Journal of organic chemistry
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Mukaiyama–Michael Reactions with Acrolein and Methacrolein: A Catalytic Enantioselective Synthesis of the C17–C28 Fragment of Pectenotoxins

2013

Enantioselective iminium-catalyzed reactions with acrolein and methacrolein are rare. A catalytic enantioselective Mukaiyama-Michael reaction that readily accepts acrolein or methacrolein as substrates, affording the products in good yields and 91-97% ee, is presented. As an application of the methodology, an enantioselective route to the key C17-C28 segment of the pectenotoxin using the Mukaiyama-Michael reaction as the key step is described.

Models MolecularMolecular StructureChemistryOrganic ChemistryAcroleinEnantioselective synthesisStereoisomerismMethacroleinBiochemistryCatalysisCatalysischemistry.chemical_compoundOrganic chemistryMarine ToxinsAcroleinPhysical and Theoretical Chemistryta116PyransOrganic Letters
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Asymmetric synthesis of α,β-diamino acid derivatives with an aziridine-, azetidine- and γ-lactone-skeleton via Mannich-type additions across α-chloro…

2012

The efficient asymmetric synthesis of new chiral γ-chloro-α,β-diamino acid derivatives via highly diastereoselective Mannich-type reactions of N-(diphenylmethylene) glycine esters across a chiral α-chloro-N-p-toluenesulfinylimine was developed. The influence of the base, LDA or LiHMDS, used for the formation of the glycine enolates, was of great importance for the anti-/syn-diastereoselectivity of the Mannich-type reaction. The γ-chloro-α,β-diamino acid derivatives proved to be excellent building blocks for ring closure towards optically pure anti- and syn-β,γ-aziridino-α-amino esters, and subsequent ring transformation into trans-3-aminoazetidine-2-carboxylic acid derivatives and α,β-diami…

Models MolecularStereochemistryAziridinesAzetidineDiamino acidRing (chemistry)BiochemistryLactoneschemistry.chemical_compoundBiosynthesisAmino AcidsPhysical and Theoretical Chemistryta116chemistry.chemical_classificationMolecular StructureSulfur CompoundsOrganic ChemistryEnantioselective synthesisStereoisomerismAziridinechemistryGlycineAzetidinesIminesChlorine CompoundsLactoneOrganic & Biomolecular Chemistry
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