Search results for "cyclic"

showing 10 items of 2439 documents

Stereoselective Conjugate Addition of Mixed Organoaluminum Reagents to ?,?-Unsaturated N-Acyloxazolidinones Derived from Carbohydrates.

2005

The stereoselective synthesis of β-branched carboxylic acid derivatives was accomplished by conjugate addition of mixed organoaluminum reagents to chiral α,β-unsaturated N-acyloxazolidinones. Mixed organoaluminum reagentswere generated in situ by transmetalation of Grignard or organolithium compounds with methylaluminum dichloride. Efficient stereocontrol was achieved using different bicyclic glycosamine-derived oxazolidinones, yielding alternatively (R)- or (S)-configured β-branched carboxylic acid derivatives.

chemistry.chemical_classificationAddition reactionTransmetalationchemistryBicyclic moleculeOrganolithium compoundsReagentCarboxylic acidOrganic chemistryStereoselectivityGeneral MedicineConjugateChemInform
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Interaction between 24-hydroxycholesterol, oxidative stress, and amyloid-β in amplifying neuronal damage in Alzheimer’s disease: three partners in cr…

2011

All three cholesterol oxidation products implicated thus far in the pathogenesis of Alzheimer's disease, 7β-hydroxycholesterol, 24-hydroxycholesterol, and 27-hydroxycholesterol, markedly enhance the binding of amyloid-beta (Aβ) to human differentiated neuronal cell lines (SK-N-BE and NT-2) by up-regulating net expression and synthesis of CD36 and β1-integrin receptors. However, only 24-hydroxycholesterol markedly potentiates the pro-apoptotic and pro-necrogenic effects of Aβ(1-42) peptide on these cells: 7β-hydroxycholesterol and 27-hydroxycholesterol, like unoxidized cholesterol, show no potentiating effect. This peculiar behavior of 24-hydroxycholesterol at physiologic concentrations (1 μ…

chemistry.chemical_classificationAgingReactive oxygen speciesbiologyCD36NeurotoxicityLong-term potentiationCell BiologyGlutathionemedicine.diseasemedicine.disease_causeCell biologychemistry.chemical_compoundchemistryBiochemistrypolycyclic compoundsbiology.proteinmedicinelipids (amino acids peptides and proteins)ReceptorOxidative stressIntracellularAging Cell
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Stereoselective Synthesis of the Glycosidase Inhibitor Australine through a One-Pot, Double-Cyclization Strategy

2006

[reaction: see text] A stereocontrolled, convergent synthesis of the alkaloid australine, a glycosidase inhibitor of the pyrrolizidine class, is described. The chiral starting materials were ketone 3, derived from L-erythrulose, and alpha-alkoxy aldehyde 4, prepared from L-malic acid. A key step of the synthesis was the highly stereoselective aldol reaction between 4 and a Z boron enolate derived from 3. Another key step was the one-pot construction of the bicyclic pyrrolizidine system by means of a three-step sequence of SN2 displacements induced by benzylamine on a trimesylate precursor.

chemistry.chemical_classificationAldehydesKetoneGlycoside HydrolasesMolecular StructureBicyclic moleculeStereochemistryOrganic ChemistryConvergent synthesisStereoisomerismKetonesBiochemistryAldehydechemistry.chemical_compoundBenzylaminechemistryAldol reactionCyclizationPyrrolizidineSN2 reactionEnzyme InhibitorsPhysical and Theoretical ChemistryPyrrolizidine AlkaloidsOrganic Letters
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ChemInform Abstract: Facile Synthesis of 2-Nitroalkanols by Tetramethylguanidine (TMG)- Catalyzed Addition of Primary Nitroalkanes to Aldehydes and A…

2010

Abstract Tetramethylguanidine-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones constitutes a practical means to perform the nitro-aldol reaction (Henry reaction). The very mild conditions employed, together with the short reaction times, make the procedure tolerant of a range of functionalities and highly versatile for the synthesis of a variety of 2-nitroalkanols.

chemistry.chemical_classificationAlicyclic compoundAddition reactionPrimary (chemistry)Nitroaldol reactionChemistryOrganic chemistryGeneral MedicineCatalysisChemInform
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Facile synthesis of 2-nitroalkanols by tetramethylguanidine (TMG)-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones

1997

Abstract Tetramethylguanidine-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones constitutes a practical means to perform the nitro-aldol reaction (Henry reaction). The very mild conditions employed, together with the short reaction times, make the procedure tolerant of a range of functionalities and highly versatile for the synthesis of a variety of 2-nitroalkanols.

chemistry.chemical_classificationAlicyclic compoundPrimary (chemistry)Nitroaldol reactionChemistryOrganic ChemistryDrug DiscoveryOrganic chemistryBiochemistryCatalysisTetrahedron Letters
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ChemInform Abstract: Aliphatic and Alicyclic Aldehydes: Synthesis by Diels-Alder Reactions with Enals or Their Acetals

2009

chemistry.chemical_classificationAlicyclic compoundchemistryStereochemistryDiels alderOrganic chemistryGeneral MedicineChemInform
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ChemInform Abstract: Diastereoselective Intramolecular Additions of Allyl- and Propargylsilanes to Iminium Ions: Synthesis of Cyclic and Bicyclic Qua…

2010

Cyclization of the chiral imino lactones with allylic or propargylic groups required acidic conditions to afford spirocyclic (II) or (XII).

chemistry.chemical_classificationAllylic rearrangementchemistryBicyclic moleculeIntramolecular forceIminiumGeneral MedicineMedicinal chemistryIonAmino acidChemInform
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Selective Transformation of Norbornadiene into Functionalized Azaheterocycles and β‐Amino Esters with Stereo‐ and Regiocontrol

2021

Novel functionalized azaheterocycles with multiple chiral centers have been accessed from readily available norbornene β-amino acids or β-lactams across a stereocontrolled synthetic route, based on ring-opening metathesis (ROM) of the staring unsaturated bicyclic amino esters, followed by selective cyclization through ring-closing metathesis (RCM). The RCM transformations have been studied under various experimental conditions to assess the scope of conversion, catalyst, yield, and substrate influence. The structure of the starting norbornene β-amino acids predetermined the structure of the new azaheterocycles, and the developed synthetic route took place with the conservation of the config…

chemistry.chemical_classificationAmino estersBicyclic moleculeNorbornadiene01.04. Kémiai tudományokOrganic ChemistryGeneral ChemistryMetathesisBiochemistryCombinatorial chemistryAmino acidCatalysischemistry.chemical_compoundchemistryYield (chemistry)NorborneneChemistry – An Asian Journal
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Evaluation and comparison of tailor-made stationary phases based on spherical silica-based beads for capillary electrochromatography via peptide sepa…

2004

Small cyclic peptides have been employed to elucidate the performance of novel sorbents as stationary phases in capillary electrochromatography (CEC). In this paper chain length dependencies for ordinary liquid chromatographic sorbents are reported together with findings acquired on beads specifically designed to suit CEC. The latter, tailor-made, spherical, porous silica exhibits a distinguished surface modification to meet the criteria anticipated to enhance performance profiles in CEC. With well-characterised peptides resembling the analytes, probing of the CEC system in a systematic manner (predominantly via the organic modifier content of the background electrolyte (BE)) reveals insigh…

chemistry.chemical_classificationAnalyteCapillary electrochromatographyChromatographySilicon dioxideClinical BiochemistryAnalytical chemistryCell BiologyGeneral MedicineElectrolyteSilicon DioxideBiochemistryCyclic peptideAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochromatographycardiovascular systemSurface modificationAmino Acid SequencePorosityPeptidesChromatography Micellar Electrokinetic CapillaryJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Synthesis of Lamellarin D Trimethyl Ether and Lamellarin H via 6π-Electrocyclization.

2015

An electrocyclic ring closure of a 2-azapentadienyl anion generated in situ from a chalcone and glycine ester is the key step of an efficient synthesis of the pyrrole core of the lamellarin alkaloids. A recently developed scalable one-pot procedure provides multigram quantities of a 3,5-diaryl-4-iodopyrrole-2-carboxylate intermediate which is transformed in four further high-yielding operations including a one-pot Pomeranz–Fritsch alkylation/cyclization and an Ullmann-type lactone ring closure into the pentacyclic lamellarin skeleton.

chemistry.chemical_classificationAnionsChalconeAlkylationMolecular StructureStereochemistryOrganic ChemistryEtherStereoisomerismStereoisomerismAlkylationRing (chemistry)IsoquinolinesHeterocyclic Compounds 4 or More Ringschemistry.chemical_compoundchemistryCoumarinsCyclizationLamellarin DPyrrolesLactonePyrroleEthersThe Journal of organic chemistry
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