Search results for "Optically active"

showing 10 items of 31 documents

Inorganic Protection of Polymer Nanocapsules: A Strategy to Improve the Efficiency of Encapsulated Optically Active Molecules

2018

chemistry.chemical_classificationChemistryLayer by layer02 engineering and technologyGeneral ChemistryPolymerOptically active010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPhoton upconversionNanocapsules0104 chemical scienceslaw.inventionChemical engineeringlawMoleculeCrystallization0210 nano-technologyIsrael Journal of Chemistry
researchProduct

Flexible Synthesis of Planar Chiral Azoninones and Optically Active Indolizidinones

2014

The flexible synthesis of defined substituted optically active indolizidinones starting from chiral pool (S)-proline and trans 4-hydroxy-(S)-proline is described. Several defined 2-vinylpyrrolidines were generated in short sequences. The aza-Claisen rearrangement using chloro and phenylketene equivalents delivered nine-membered-ring lactams with up to three stereogenic centres and pS-arranged E olefins. Depending on the substitution pattern, certain azoninones had a flexible conformation and showed pS/pR double-bond flipping. Treatment of the unsaturated lactams with the soft electrophile iodine induced diastereoselective transannular ring contractions. Here, the planar chiral arrangement o…

chemistry.chemical_classificationPlanarDouble bondchemistryStereochemistryOrganic ChemistryElectrophileMoleculePhysical and Theoretical ChemistrySigmatropic reactionOptically activeRing (chemistry)StereocenterEuropean Journal of Organic Chemistry
researchProduct

ChemInform Abstract: Tandem Asymmetric Michael Reaction-Intramolecular Michael Addition. An Easy Entry to Chiral Fluorinated 1,4-Dihydropyridines.

2010

The sequential treatment of optically active sulfoxide (I) with fluorinated nitriles and alkyl propiolates affords (sulfinylmethyl)dihydropyridines of type (IV) as single diastereomers in most cases.

chemistry.chemical_classificationchemistry.chemical_compoundTandemchemistryIntramolecular forceMichael reactionDiastereomerSulfoxideGeneral MedicineOptically activeMedicinal chemistrySequential treatmentAlkylChemInform
researchProduct

1,2-Asymmetric Induction in Diastereo­selective Zwitterionic Aza-Claisen Rearrangements: Key Steps in Optically Active Alkaloid Synthesis

2013

The zwitterionic aza-Claisen rearrangement of optically active N-allylpyrrolidines and α-phenoxyacetyl fluorides proceeds with complete simple diastereoselectivity (internal asymmetric induction) and complete 1,2-asymmetric induction to generate a new C–C bond adjacent to a chiral C-N-Boc functionality. The resulting γ,δ-unsaturated amides were cyclised to give the corresponding pyrrolizidinones, which enabled the determination of the relative configuration of the stereotriads. Vinyl group degradation and a final lactam reduction gave an optically active analogue of (+)-petasinine (a pyrrolizidine alkaloid). Furthermore, the stereotriad-containing amides should be useful key intermediates f…

chemistry.chemical_compoundPyrrolizidine alkaloidChemistryStereochemistryOrganic ChemistryAlkaloid synthesisLactamTotal synthesisIndolizidinePhysical and Theoretical ChemistryOptically activeAsymmetric inductionEuropean Journal of Organic Chemistry
researchProduct

ChemInform Abstract: A New Tandem Cross Metathesis-Intramolecular Aza-Michael Reaction for the Synthesis of α,α-Difluorinated Lactams.

2012

Difluorinated amides are treated with methyl vinyl ketone or analogous esters to produce the desired γ- and δ-lactam units including optically active versions.

chemistry.chemical_compoundTandemChemistryIntramolecular forceMethyl vinyl ketoneMichael reactionSalt metathesis reactionOrganic chemistryGeneral MedicineOptically activeMetathesisPyrrole derivativesChemInform
researchProduct

Kinetische Racematspaltungen ausgehend vonrac-Alkoholen oderrac-Carbonsäurehalogeniden unter Mitwirkung optisch aktiver Induktorbasen

1989

Bei der Umsetzung eines Molaquivalents achiraler Carbonsaurehalogenide mit zwei Molaquivalenten rac-Alkoholen entstehen unter Mitwirkung von einem Molaquivalent einer optisch aktiven Induktorbase (tertiares Amin) partiell optisch aktive Ester sowie partiell optisch aktive Alkohole in zum Teil hoher optischer Reinheit (60 – 70%). Der im Ester gebundene Anteil an Alkohol sowie der nicht umgesetzte Alkohol haben entgegengesetzte Konfiguration. Der Induktionsgrad ist ahnlich hoch, wenn man zwei Molaquivalente eines rac-Carbonsaurehalogenids mit je einem Molaquivalent eines achiralen Alkohols und einer Induktorbase umsetzt. Der Carbonsaureanteil im Ester und die freie Saure haben entgegengesetzt…

chemistry.chemical_compoundTertiary amineStereochemistryChemistryOrganic ChemistryMoietyAlcoholPhysical and Theoretical ChemistryOptically activeEnantiomeric excessLiebigs Annalen der Chemie
researchProduct

An efficient entry to optically active anti- and syn-beta-amino-alpha-trifluoromethyl alcohols.

2008

The reaction of chiral 5,6-dihydro-2H-1,4-oxazin-2-ones with TMSCF3 in the presence of a suitable activator leads to trifluoromethyl lactols, which can be selectively reduced to anti-beta-amino-alpha-trifluoromethyl alcohols. The corresponding syn diastereoisomers are obtained when the starting imines are reduced and the nitrogen atom is conveniently protected. In addition, a novel rearrangement of the CF3 group in the lactol intermediates has been observed. This represents a formal CF3 addition to the imine function in the starting substrates.

chemistry.chemical_compoundTrifluoromethylNitrogen atomStereochemistryChemistryLactolOrganic ChemistryImineDiastereomerPhysical and Theoretical ChemistryOptically activeBiochemistryOrganic letters
researchProduct

Studien zum Vorgang der Wasserstoffübertragung, 41. Elektroreduktion von Acetophenon unter Mitwirkung optisch aktiver Leitsalze

1977

Die Anderung des Carbinol/Pinakol-Verhaltnisses2) (C/P) und der optischen Induktion bei der Elektroreduktion von Acetophenon mit (1 R, 2S)-N-(3-Cyanpropyl)-N-methylephedriniumbromid (1) und (1 R, 2 S)-N,N-Dimethylephedriniumbromid (2) als Leitsalze wird untersucht in Abhangigkeit: a) vom Potential (Tabelle 1), b) von der Stromdichte (Tabelle 2), c) von Pulsbedingungen (Tabelle 3), d) vom pH (Tabelle 4), e) von der Anwesenheit anderer Kationen (Tabelle 5), f) vom Losungsmittel (Tabelle 6), g) von der Temperatur (Tabelle 7) und h) von der Art des Elektrodenmaterials (Tabelle 8). — Es werden tensammetrische und cyclovoltammetrische Messungen durchgefuhrt. Die in trockenem Dimethylformamid erha…

chemistry.chemical_compoundchemistryBromideSupporting electrolyteOrganic ChemistryHydrogen transferDimethylformamidePhysical and Theoretical ChemistryOptically activeCyclic voltammetryMedicinal chemistryAcetophenoneJustus Liebigs Annalen der Chemie
researchProduct

Racemattrennung, Kristallstruktur und histaminartige Wirkung von 4-[1-(2-Aminoethylthio)ethyl]-5-methylimidazol

1983

Es wird die Racemattrennung von 4-[1-(2-Aminoethylthio)ethyl]-5-methylimidazol (1) mittels optisch aktiver Di-O-(p-toluoyl)weinsaure sowie die histaminartige Wirksamkeit der Enantiomeren beschrieben. Von (+)-1 · 2HCl · H2O wurde die Kristallstruktur bestimmt und bis zu einem R-Wert von 0.0483 verfeinert. Danach ist (+)-1R-konfiguriert. Von den beiden Enantiomeren besitzt nur (S)-(−)-1 H1-agonistische Aktivitat. Resolution, Crystal Structure, and Histamine-like Activity of 4-[1-(2-Aminoethylthio)ethyl]-5-methylimidazole The resolution of racemic 4-[1-(2-aminoethylthio)ethyl]-5-methylimidazole (1) using optically active Di-O-(P-toluoyl)tartaric acid as well as the histamine-like activity of t…

chemistry.chemical_compoundchemistryOrganic ChemistryResolution (electron density)Tartaric acidCrystal structurePhysical and Theoretical ChemistryEnantiomerOptically activeMedicinal chemistryLiebigs Annalen der Chemie
researchProduct

New Optically Active 4-Alkoxyprolinol Ethers Derived from trans-4-Hydroxy-L-proline

2011

(2S,4R)-trans-4-Hydroxy-L-proline has been used as thechiral-pool source in the efficient syntheses of optically active protected 4-hydroxyprolinols. After N-acyl protection andester formation, the first ether moiety was introduced maintaining the chiral centre adjacent to the ester. Then, reduction of the ester delivered the corresponding carbinol, which had to be alkylated selectively to avoid side reactions with the N-protecting group. Finally, the N-acyl function was removed to generate the target methyl and tert-butyl ethers displaying defined substitution patterns. The so-formed optically active 4-alkoxyprolinol ethers can be used as core fragments in biologically active compounds or …

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistryEnantioselective synthesisMoietyEtherBiological activityPhysical and Theoretical ChemistryOptically activeAlkylationTrans-4-Hydroxy-L-prolineEuropean Journal of Organic Chemistry
researchProduct