Search results for "Amide"

showing 10 items of 3119 documents

ChemInform Abstract: Synthesis and Stereochemical Studies of 2-Substituted Thiazolidine-4-carboxamide Derivatives.

2010

A series of new 2-substituted thiazolidine-4-carboxamide derivatives which have potentially useful immunological properties, have been synthesized in a stereoselective manner by coupling 2-subsituted thiazolidine-4-carboxylic acids with amines or amino esters. The structure of these compounds was established by combination of NMR methods and by X-ray analysis.

chemistry.chemical_compoundchemistryAmino estersmedicine.drug_classStereochemistryThiazolidinemedicineCarboxamideStereoselectivityGeneral MedicineCombinatorial chemistryChemInform
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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
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1967

Enamines derived from cyclic ketones behave as difunctional intermediates when treated with phenyl isocyanate to produce dicarboxanilides. Reaction of bis(4-isocyanatophenyl)-methane with 1-N-morpholino-1-cyclopentene in DMSO leads to poly[iminocarbonyl(2-morpholino-1-cyclopenten-1.3-ylene)carbonylimino-p-phenylenemethylene-p-phenylene], a polyamide. The effects of various cyclic enamines and diisocyanates on the polymerization are surveyed. Morpholine and piperidine are more effective than pyrrolidine or dimethylamine when incorporated into cyclopentanone enamines. The molecular weight of the polymer decreases when the ring size of the ketone component is increased. The efficiency of the d…

chemistry.chemical_compoundchemistryMorpholinePolyketonePolymer chemistryPolyamideHexamethylene diisocyanatePiperidineCyclopentanonePyrrolidineEnamineDie Makromolekulare Chemie
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N-(Diphenylmethylene)benzenesulfonamide andN-(Diphenylmethylene)-4-methylbenzenesulfonamide

2008

[10398-99-9] C19H15NO2S (MW 332.42) InChI = 1S/C19H15NO2S/c21-23(22,18-14-8-3-9-15-18)20-19(16-10-4-1-5-11-16)17-12-6-2-7-13-17/h1-15H InChIKey = LECLPBHPQOFADH-UHFFFAOYSA-N (reagent used as an activated imine) Physical Data: mp 119–120 °C. Form Supplied in: colorless crystals. Not commercially available. Purification: recrystalization from CH3OH. [10399-00-5] C20H17NO2S (MW 346.45) InChI = 1S/C20H17NO2S/c1-16-12-14-19(15-13-16)24(22,23)21-20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3 InChIKey = ODLFJRFKAOOIKO-UHFFFAOYSA-N (reagent used as an activated imine) Physical Data: mp 103–104 °C1; 102–103 °C2; 101–102 °C5; 103 °C6; 102–104 °C.7 Solubility: soluble in pyridine, dimethylformamide, …

chemistry.chemical_compoundchemistryReagentIminePyridineOrganic chemistryDimethylformamideSolubilityBenzeneAcetonitrileMedicinal chemistryTetrahydrofuran
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ChemInform Abstract: STRUKTUR-WIRKUNGS-BEZIEHUNGEN BEI ANALEPTICA VOM TYP DES NICETHAMIDS 3. MITT. SYNTHESE VON ANALOGEN DES 6-METHYL-NICETHAMIDS

1975

Als potentiell analeptisch wirksame Substanzen mit partiell fixierter funktioneller Gruppe werden strukturanaloge Amide, Imide und Lactame des 2-Methyl-nicethamids synthetisiert. Synthesis of 2-Methyl-Nicethamide Analogues. As potentially analeptically active substances with partially fixed functional groups, structural analogues of 2-methyl-nicethamide, in the form of amides, imides and lactams, are synthesized.

chemistry.chemical_compoundchemistryStereochemistryAmideGeneral MedicineImideChemischer Informationsdienst
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Zwitterionic Aza-Claisen Rearrangements Controlled by Pyrrolidine Auxiliaries - Useful Key Steps in Convergent Enantioselective Syntheses

2012

Chiral pyrrolidine substituents served as efficient auxiliaries in diastereoselective zwitterionic ketene aza-Claisen rearrangements. Palladium-catalysed N-allylation starting from optically active proline and prolinol derivatives, as well as from (2S,5S)-2,5-dimethoxymethylpyrrolidine, gave various allylamines bearing trisubstituted olefin moieties. Treatment with complex carboxylic acid fluorides in the presence of trimethylaluminium induced activated ketene addition to the nitrogen and subsequent [3,3] sigmatropic rearrangement to give γ,δ-unsaturated amides with excellent simple diastereoselectivities and up to 11:1 auxiliary-induced diastereomeric ratios. Cleavage of the pyrrolidine am…

chemistry.chemical_compoundchemistryStereochemistryAmideOrganic ChemistryIodolactonizationEnantioselective synthesisDiastereomerKetenePhysical and Theoretical ChemistrySigmatropic reactionPyrrolidineProlinolEuropean Journal of Organic Chemistry
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Transamidation reactions of 2-(2-sulfonylguanidino)acetamides

2007

Abstract The reactivity of a series of sulfonylguanidinoacetamides 2A–E towards amines is reported. Guanidinoacetamides 2A–C, containing the arylsulfonylimino moiety, undergo a facile transamidation to give substituted carboxamides 4A–C, through the imidazolidinone intermediate 3. Acetamide 2D, having a methanesulfonylimino substituent, affords the imidazolidinone 3D and no transamidated carboxamides 4 are detected. In the case of guanidinoacetamide 2E, with a p-nitrobenzenesulfonylimino substituent, a Smiles rearrangement was observed.

chemistry.chemical_compoundchemistryStereochemistryImidazolidinoneOrganic ChemistryDrug DiscoverySubstituentMoietyReactivity (chemistry)Smiles rearrangementBiochemistryAcetamideTetrahedron
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NMR-Spektroskopie an Heterocyclen, 3. Mitt.: Homologe, vinyloge und kernalkylierte Nicethamidanaloge

1976

Von homologen, vinylogen und kernalkylierten Nicethamidanalogen wurden die 13C-NMR-Shiftwerte ermittelt und mit Hilfe der 1H-NMR-Spektroskopie durch Koaleszenzbestimmung die Energiebarriere bei der gehinderten Rotation der Amidgruppe bestimmt. Homologous, Vinylogous, and Ring Alkylated Nicethamide Analogs The 13C-NMR shifts were determined for homologous, vinylogous and ring alkylated nicethamide analogs and the energy barrier of the hindered rotation of the amide group was evaluated by means of coalescence measurements with 1H-NMR.

chemistry.chemical_compoundchemistryStereochemistryNicethamideAmideDrug DiscoveryPharmaceutical ScienceAlkylationRing (chemistry)Archiv der Pharmazie
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The bleaching efficacy of carbamide peroxide gels containing potassium nitrate desensitizer

2020

Background To evaluate the bleaching efficacy of at-home carbamide peroxide (CP) gels in two concentrations, containing or not a desensitizing agent. Material and methods Forty incisors were divided into four groups (n=10), according to gel concentrations (10% or 22%), and presence or not of 3% potassium nitrate in the gel. A thin layer of gel was applied to the buccal surface of each tooth for 2h/day for 4 weeks. Bleaching efficacy was measured using a spectrophotometer, and ∆E*ab, ∆E00 and ∆WID were calculated. Measurements were performed at baseline, 7, 14, 21, 28, and 35 days following the first gel application. Data were analyzed by two-way RM-ANOVA and Tukey's test (α=0.05). Results R…

chemistry.chemical_compoundgenetic structureschemistryResearchThin layerUNESCO::CIENCIAS MÉDICASPotassium nitrateEsthetic DentistryCarbamide peroxidePositive correlation:CIENCIAS MÉDICAS [UNESCO]General DentistryNuclear chemistry
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Electrochemical and bioelectrocatalytical properties of novel block-copolymers containing interacting ferrocenyl units

2008

The electrochemical characterization of three different polystyrene-b-polybutadiene block-copolymers, functionalized with diferrocenylsilane units, is reported. The PB-blocks have been functionalized with different fractions of electronicall y communicated, PSm-PB„ p (HSiMeFc2)p units, where m = 615, n = 53, p = 39 (1), m = 375, n = 92, p = 76 (2) and m = 455, n = 204, p = 170 (3). Electrochemical character­ ization has been carried out both in solution and after electrochemical deposition onto platinum electrodes. The bioelectrocatalytical properties of electrodes modified with the polymers in the nicotinamide dinucleotide (NADH) and glucose oxidase (GOx) oxidations have been investigated …

chemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerGlucose oxidasePhysical and Theoretical Chemistrychemistry.chemical_classificationNicotinamidebiologyChemistryOrganic ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciencesFerroceneElectrodebiology.protein0210 nano-technologyPlatinumJournal of Organometallic Chemistry
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