Search results for "selective synthesis"

showing 10 items of 430 documents

ChemInform Abstract: Enantioselective Mannich Reaction of β-Keto Esters with Aromatic and Aliphatic Imines Using a Cooperatively Assisted Bifunctiona…

2015

The title reaction tolerates aliphatic and aromatic substituents on both reaction partners, affording products (III) as a mixture of inseparable diastereomers with low or without any diastereoselectivity.

ChemistryOrganocatalysisEnantioselective synthesisDiastereomerOrganic chemistryGeneral MedicineMannich reactionBifunctional catalystChemInform
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Organocatalytic asymmetric addition of naphthols and electron-rich phenols to isatin-derived ketimines: highly enantioselective construction of tetra…

2015

A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols and activated phenols to ketimines derived from isatins. The reaction afforded chiral 3-amino-2-oxindoles with a quaternary stereocenter in high yields (up to 99%) with excellent enantioselectivity (up to 99% ee). To the best of our knowledge, this transformation is the first highly enantioselective addition of naphthols to ketimines

ChemistryOrganocatalysisIsatinIsatin-derived ketiminesEnantioselective synthesisAsymmetric synthesisGeneral ChemistryNaphtholsGeneral MedicineCatalysisStereocenterReaccions químiqueschemistry.chemical_compoundThioureaCatàlisiOrganocatalysisFISICA APLICADAOrganic chemistryPhenolsFriedel-Crafts reactionsQuímica orgànicaAngewandte Chemie (International ed. in English)
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Asymmetric Synthesis of Dihydropyranones with Three Contiguous Stereocenters by an NHC‐Catalyzed Kinetic Resolution

2021

An oxidative NHC-catalyzed kinetic resolution (KR) of racemic mixtures is presented. The developed reaction furnishes tricyclic dihydropyranones with three contiguous stereocenters in excellent dia- and enantioselectivity, with good-to-moderate yields. Mechanistic studies indicate that the rate-determining step of the reaction is the formation of the Breslow intermediate, while the selectivity determining step occurs later in the mechanism. The presented methodology enables rapid synthesis of complex structures in a single step.

ChemistryOrganocatalysisOrganic ChemistryEnantioselective synthesisSingle stepPhysical and Theoretical ChemistrySelectivityCombinatorial chemistryCatalysisKinetic resolutionStereocenterEuropean Journal of Organic Chemistry
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Asymmetric Methods for Carbon‐Fluorine Bond Formation

2021

ChemistryOrganocatalysisOrganic ChemistryPolymer chemistryCarbon–fluorine bondEnantioselective synthesisFluorinechemistry.chemical_elementPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Catalytic Enantioselective α-Oxysulfonylation of Ketones Mediated by Iodoarenes

2008

The alpha-oxysulfonylation of ketones catalysed by enantioenriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity. We believe this to be the first report of an enantioselective organocatalytic reaction involving hypervalent iodine reagents which should open up a new field for enantioselective organocatalysis of oxidation reactions.

ChemistryOrganocatalysisReagentYield (chemistry)Organic ChemistryEnantioselective synthesisHypervalent moleculeOrganic chemistryPhysical and Theoretical ChemistryRedoxStoichiometryCatalysisEuropean Journal of Organic Chemistry
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Enantioselective Synthesis of P-Chirogenic Phosphorus Compounds via the Ephedrine-Borane Complex Methodology

2008

The stereoselective synthesis of P-chirogenic organophosphorus compounds using the versatile ephedrine-methodology is reported. The principle of the method is based on the diastereoselective preparation of 1,3,2-oxazaphospholidine borane 3 from ephedrine 2 and regio- and stereoselective ring-opening of the heterocycle leading to an aminophosphine borane 4. Finally, these ring-opening products 4 are easily transformed into P-chirogenic organophosphorus compounds, by subsequent highly stereoselective reactions involving electrophilic or nucleophilic strategies.

ChemistryPhosphorusOrganic ChemistryEnantioselective synthesischemistry.chemical_elementBoraneBiochemistryInorganic Chemistrychemistry.chemical_compoundNucleophileElectrophilemedicineOrganic chemistryStereoselectivityEphedrinemedicine.drugPhosphorus, Sulfur, and Silicon and the Related Elements
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Exploring the potential of some yeast strains in the stereoselective synthesis of aldol reaction products and its reduced 1,3-dialcohol derivatives

2013

Abstract The behavior of two yeast strains has been studied under different conditions. Both microorganims catalyzed the aldol reaction between activated aldehydes and acetone when a large amount of the latter was present in the reaction medium producing, with moderate stereoselectivity, the aldol product with the R configuration. No reduction of any of the products present in the medium was detected. On the other hand, the carbonyl group of the racemic aldol was reduced to produce chiral 1,3-dialcohol derivatives when water was employed as the only solvent. In this case, the resolution of the racemic starting material was also possible with one of the biocatalysts, and the aldol was recove…

ChemistryProcess Chemistry and TechnologyCarbonyl reductionEnantioselective synthesisBioengineeringBiochemistryCatalysisLewis acid catalysisStereocenterAldol reactionBiocatalysisOrganic chemistryAldol condensationStereoselectivityJournal of Molecular Catalysis B: Enzymatic
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ChemInform Abstract: Synthesis of Pyrrolidin-2-ones and of Staurosporine Aglycon (K-252c) by Intermolecular Michael Reaction.

2010

Indolo[2,3-a]pyrrolo[3,4-c]carbazoles were isolated from nature, e.g., from low plants, especially fungi, as structurally rare natural substances. Responsible for naming and also the most important representative of this type is staurosporine (1), isolated from Streptomyces staurosporeus, and its aglycon (2), also known as staurosporinone or K-252c. 3,4-Disubstituted pyrrolidin-2-ones, a group of compounds with many interesting biological properties are related to staurosporinone. The most important property is the inhibition of protein kinase C (PKC), so that this antiproliferative agent can interfere with the cell cycle. The synthetic strategy, developed by us, allows the synthesis of pyr…

ChemistryStereochemistryIntermolecular forceEnantioselective synthesisGeneral Medicinechemistry.chemical_compoundBiological propertyNitroMichael reactionLactammedicineStaurosporineProtein kinase Cmedicine.drugChemInform
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ChemInform Abstract: Base-Dependent Stereodivergent Intramolecular Aza-Michael Reaction: Asymmetric Synthesis of 1,3-Disubstituted Isoindolines.

2014

For the reaction of the compounds (I) the careful choice of the base allows the exclusive formation of either cis or trans diastereoisomer with the exception of the trihalogenates (Ie) and (If), which afford the cis-products regardless of the base used.

ChemistryStereochemistryIntramolecular forceEnantioselective synthesisMichael reactionDiastereomerGeneral MedicineBase (exponentiation)ChemInform
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Organocatalytic Enantioselective Intramolecular (Hetero)Michael Additions in Desymmetrization Processes

2021

ChemistryStereochemistryIntramolecular forceOrganocatalysisOrganic ChemistryEnantioselective synthesisPhysical and Theoretical ChemistryDesymmetrizationEuropean Journal of Organic Chemistry
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