Search results for "desymmetrization"

showing 10 items of 14 documents

Frontispiece: Recent Advances in Enantioselective Desymmetrizations of Prochiral Oxetanes

2021

chemistry.chemical_compoundChemistryOrganic ChemistryEnantioselective synthesisOrganic chemistryGeneral ChemistryOxetaneDesymmetrizationCatalysisChemistry – A European Journal
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Silver Oxide Mediated Monotosylation of Poly(ethylene glycol) (PEG): Heterobifunctional PEG via Polymer Desymmetrization

2017

Heterobifunctional poly(ethylene glycol)s (PEGs) are key structures for bioconjugation in the context of the “PEGylation” strategy to enhance blood circulation times of, for example, peptide drugs or “stealth” liposomes. The formation of heterobifunctional PEGs from symmetric PEG diols is challenging because of limited yields of the targeted monofunctional product and difficulties associated with separation steps. On the basis of a detailed comparison of reaction conditions, we have investigated a “polymer desymmetrization” strategy to maximize the yields of monofunctional PEG tosylate. The tosylation reaction in the presence of the heterogeneous catalyst silver oxide and potassium iodide i…

BioconjugationPolymers and PlasticsOrganic Chemistrytechnology industry and agricultureContext (language use)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesDesymmetrization0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPEG ratioPolymer chemistryMaterials ChemistryPEGylation0210 nano-technologyEthylene glycolSilver oxideMacromolecules
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Recent Advances in Enantioselective Desymmetrizations of Prochiral Oxetanes

2021

Abstract Strain relief of oxetanes offers a plethora of opportunities for the synthesis of chiral alcohols and ethers. In this context, enantioselective desymmetrization has been identified as a powerful tool to construct molecular complexity and this has led to the development of elegant strategies on the basis of transition metal, Lewis acid, and Brønsted acid catalysis. This review highlights recent examples that harness the inherent reactivity of prochiral oxetanes and offers an outlook on the immense possibilities for synthetic application.

Molecular complexity010405 organic chemistryChemistryOrganic Chemistryoxetaneoxygen heterocyclesEnantioselective synthesisMinireviewsContext (language use)General ChemistryStrain relief010402 general chemistry01 natural sciencesCombinatorial chemistryDesymmetrizationCatalysis0104 chemical sciencesdesymmetrizationstrained moleculesMinireviewLewis acids and basesAsymmetric SynthesisChemistry – A European Journal
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Biferrocene Amino Acid, a Ferrocenylogoue of Ferrocene Amino Acid: Synthesis, Cross-Linking, and Redox Chemistry

2010

Access of the novel biferrocene amino acid 7 is provided by two different routes, namely, via desymmetrization of a biferrocene and via palladium-catalyzed cross-coupling of two substituted ferrocenes. The dissymmetric biferrocene 7 is head−head coupled to ureylene-bridged bis(biferrocene) 9 and also head−tail coupled to amide-bridged bis(biferrocene) 14. The monomer 7 and the dimers 9 and 14 are oxidized to mixed-valent cations 7+, 9+, 92+, and 142+. The valencies are trapped in the solid state as shown by Mossbauer and EPR spectroscopy and by X-ray diffraction analysis of [7](I3). Paramagnetic NMR shift studies (7 → 7+) suggest that the hole is localized at the N-substituted ferrocene uni…

Valence (chemistry)StereochemistryOrganic ChemistryDesymmetrizationRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographyMonomerchemistryFerrocenelawMössbauer spectroscopyPhysical and Theoretical ChemistryElectron paramagnetic resonanceOrganometallics
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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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Asymmetric Synthesis of Spiro β-Lactamsviaa Squaramide- Catalyzed Sulfa-Michael Addition/Desymmetrization Protocol

2016

An efficient asymmetric synthesis of spirocyclohexenone β-lactams bearing three contiguous stereocenters has been achieved in moderate to good yields and high stereoselectivities. The protocol involves the combination of a squaramide-catalyzed sulfa-Michael addition under desymmetrization via a dynamic kinetic resolution of racemic 2,5-cyclohexadienones.

010405 organic chemistryChemistryStereochemistrybeta-lactamsasymmetric synthesisEnantioselective synthesisSquaramideGeneral Chemistry010402 general chemistry01 natural sciencesDesymmetrization0104 chemical sciencesKinetic resolutionStereocenterCatalysisOrganocatalysisMichael reactionta116Advanced Synthesis & Catalysis
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Stereoselective Synthesis of Enantiomerically Pure Piperidine Derivatives by N-Galactosylation of Pyridones.

2004

Stereoselective desymmetrization of 4-pyridone has been achieved through selective N-galactosylation, activation of the N-(galactosyl)pyridone by O-silylation and immediate addition of Grignard compounds. Chiral piperidine derivatives, e.g. (S)-(+)-coniine and (5S,9S)-(+)-indolozidine 167B, were synthesised in enantiomerically pure form using these highly regio- and stereoselective reactions. After N-galactosylation of 2-pyridone and O-silylation of the N-galactosyl-2-pyridone, addition of a Grignard compound proceeded with high 1,4-regioselectivity and complete diastereoselectivity, to furnish 4-substituted 5,6-dehydro-2-piperidones. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Ger…

chemistry.chemical_compoundStereochemistryChemistryStereoselectivityGeneral MedicinePiperidineDesymmetrizationChemInform
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Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition

2018

The first example of an N-heterocyclic carbene-catalyzed asymmetric desymmetrization of enal-tethered cyclohexadienones via an intramolecular homoenolate Michael addition/esterification reaction is described. This new protocol offers a direct entry to various functionalized tetrahydrofluorenones with three contiguous stereocenters in high yields, good diastereoselectivities and excellent enantioselectivities.

aromaattiset yhdisteet010402 general chemistry01 natural sciencesDesymmetrizationCatalysisStereocenterCatalysisDirect entryMaterials Chemistryta116kemiallinen synteesi010405 organic chemistryChemistryaromatic compoundsMetals and AlloysEnantioselective synthesisGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIntramolecular forceCeramics and CompositesMichael reactionEsterification reactionchemical synthesisChemical Communications
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Stereoselective Synthesis of Enantiomerically Pure Piperidine Derivatives byN-Galactosylation of Pyridones

2004

Stereoselective desymmetrization of 4-pyridone has been achieved through selective N-galactosylation, activation of the N-(galactosyl)pyridone by O-silylation and immediate addition of Grignard compounds. Chiral piperidine derivatives, e.g. (S)-(+)-coniine and (5S,9S)-(+)-indolozidine 167B, were synthesised in enantiomerically pure form using these highly regio- and stereoselective reactions. After N-galactosylation of 2-pyridone and O-silylation of the N-galactosyl-2-pyridone, addition of a Grignard compound proceeded with high 1,4-regioselectivity and complete diastereoselectivity, to furnish 4-substituted 5,6-dehydro-2-piperidones. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Ger…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryOrganic chemistryStereoselectivityPiperidinePhysical and Theoretical ChemistryDesymmetrizationEuropean Journal of Organic Chemistry
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Asymmetric Intramolecular Aza-Michael Reaction in Desymmetrization Processes. Total Synthesis of Hippodamine and epi-Hippodamine

2015

The use of chiral sulfinyl amines both as nucleophilic nitrogen sources and chiral inducers has been described for the first time in a desymmetrization-type process involving an intramolecular aza-Michael reaction. The resulting product was employed as an advanced intermediate in the total synthesis of the natural product hippodamine and epi-hippodamine, taking advantage of the special symmetry of these molecules. In addition, this is the first asymmetric total synthesis of epi-hippodamine.

Natural productStereochemistryOrganic ChemistryTotal synthesisHippodamineBiochemistryDesymmetrizationchemistry.chemical_compoundchemistryNucleophileIntramolecular forceMichael reactionMoleculePhysical and Theoretical ChemistryOrganic Letters
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