Search results for "405"

showing 10 items of 3208 documents

Synthesis of Symmetric Ethers Using Monocationic and Dicationic Acidic Ionic Liquids

2018

A series of monocationic and dicationic -SO3H functionalized Brønsted acidic ionic liquids (BAILs) are synthesized using different amines int.al., N,N,N′,N′-tetramethylethylenediamine, 1-methylimidazole, pyridine and alkylating agents 1,3-propane- and 1,4-butanesultones. The Hammett acidity (H0) and thermal properties by TG-DSC techniques are investigated. These ionic liquids have been applied to catalyze the dehydration reaction of aliphatic long chain alcohols (1-heptanol, 1-octanol, 1-decanol) at 195 °C. The optimization of reaction conditions and use of dicationic ionic liquids allow to reach rather high yields of symmetric diheptyl ether and dioctyl ether. The reusability of ionic liqu…

chemistry.chemical_compound010405 organic chemistryMechanics of MaterialsChemistryMechanical EngineeringPolymer chemistryIonic liquidGeneral Materials Science010402 general chemistry01 natural sciences0104 chemical sciencesKey Engineering Materials
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Mild and efficient 64Cu labeling of perhydro-1, 4-diazepine derivatives for potential use with large peptides, proteins and antibodies

2020

Abstract DATA (6-Amino-1,4-diazapine-triacetate) and AAZTA (6-Amino-1,4-diazapine-tetracetate) chelators represent a novel approach representing hybrid-chelates: possessing significant cyclic and acyclic character. It is believed that flexibility of the acyclic part facilitates rapid complexation, whilst the preorganized cyclic part minimizes the energy barrier to complexation and inhibits decomplexation processes. So far, these chelators have been used exclusively with 44Sc and 68Ga only. Recent results with natCu predict high stabilities for Cu-AAZTA, yet no radioactive labeling of AAZTA or DATA with 64Cu or any additional radioactive isotope has been reported. We present the one pot synt…

chemistry.chemical_compoundDiazepinechemistrybiology010405 organic chemistrybiology.proteinPhysical and Theoretical ChemistryAntibody010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesRadiochimica Acta
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Absolute Configuration Determination of 2,3-Dihydro-1H,5H-pyrazolo[1,2-a]pyrazoles Using Chiroptical Methods at Different Wavelengths

2016

A correlation between the absolute configuration and chiroptical properties of nonracemic 1,6,7-trisubstituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazoles was studied. A series of 16 novel representatives were prepared by Cu-catalyzed [3 + 2] cycloadditions of racemic (Z)-2-benzylidene-5-oxopyrazolidin-2-ium-1-ides to tert-butyl (S)-(3-oxopent-4-yn-2-yl)carbamate, and their structures were determined by NMR, VCD, ECD, and X-ray diffraction. A clear correlation between the sign of specific rotation and configuration at position C(1) allows for easy determination of the absolute configuration of 1,6,7-trisubstituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazoles by ECD and NMR. While VCD, requirin…

chemistry.chemical_compoundWavelength010405 organic chemistryChemistryStereochemistryOrganic ChemistryAbsolute configurationPhysical chemistrySpecific rotation010402 general chemistry01 natural sciences0104 chemical sciencesSign (mathematics)The Journal of Organic Chemistry
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Pyrene-fused bisphenazinothiadiazoles with red to NIR electroluminescence

2017

The synthesis and characterisation of two pyrene-fused phenazinothiadiazole derivatives with different substituents is described. Light-emitting diodes incorporating such derivatives display red to near-infrared electroluminescence with emission peaks at wavelengths as long as 721 nm, illustrating that pyrene-fused bisphenazinothiadiazoles can serve as deep red and NIR emitters.

chemistry.chemical_compoundWavelengthchemistry010405 organic chemistryOrganic ChemistryAnalytical chemistryPyreneElectroluminescence010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesDiodeOrganic Chemistry Frontiers
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Anodic Formation of Aryl Mesylates through Dehydrogenative Coupling Reaction

2018

chemistry.chemical_compoundchemistry010405 organic chemistryArylElectrochemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisCoupling reaction0104 chemical sciencesAnodeChemElectroChem
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Understanding the Intramolecular Diels-Alder Reactions of N-Substituted N-Allyl-Furfurylamines: An MEDT Study

2017

chemistry.chemical_compoundchemistry010405 organic chemistryFuranIntramolecular forceDiels alderGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesChemistrySelect
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From One-Pot NH-Sulfoximidations of Thiophene Derivatives to Dithienylethene-Type Photoswitches

2019

Thiophene NH-sulfoximines have been synthesized using a one-pot NH-sulfoximidation reaction of thiophenes. The reactivity of the products was investigated, and the developed protocols were used for the synthesis of a new class of dithienylethene-type photoswitches containing a sulfoximidoyl group.

chemistry.chemical_compoundchemistry010405 organic chemistryOrganic ChemistryThiopheneOrganic chemistryReactivity (chemistry)Physical and Theoretical Chemistry010402 general chemistry01 natural sciencesBiochemistryThiophene derivatives0104 chemical sciencesOrganic Letters
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Efficient and stereodivergent electrochemical synthesis of optically pure menthylamines.

2011

chemistry.chemical_compoundchemistry010405 organic chemistryOrganic chemistryGeneral Chemistry010402 general chemistryOximeElectrochemistry01 natural sciencesReductive aminationCatalysis0104 chemical sciencesAngewandte Chemie (International ed. in English)
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Recent Advances in the Synthesis of Piperidines: Functionalization of Preexisting Ring Systems

2018

Abstract The present review focuses on strategies for the construction of piperidines which have appeared in the literature since 2003 through mid-2017. In a preceding chapter ( 2017AHC191 ), we summarized synthetic methods involving the construction of the piperidine ring from essentially acyclic starting materials in an intra- or intermolecular manner. The present chapter aims at giving a general overview of decoration or modification of previously generated pyridines or piperidines. The hydrogenation of preformed pyridine or pyridinium rings and introduction of substituents into fully saturated piperidines as well as ring expansion of pyrrolidines to piperidines are the most prevalent me…

chemistry.chemical_compoundchemistry010405 organic chemistryPyridineIntermolecular forceSurface modificationPyridiniumPiperidine010402 general chemistryRing (chemistry)01 natural sciencesCombinatorial chemistry0104 chemical sciences
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Asymmetric Synthesis of Five-Membered Spiropyrazolones via N-Heterocyclic Carbene (NHC)-Catalyzed [3+2] Annulations

2016

A new synthetic strategy for the asymmetric synthesis of five-membered spiropyrazolones via N-heterocyclic carbene-catalyzed [3+2] annulations employing enals and unsaturated pyrazolones as substrates has been developed. The new protocol allows the flexible variation of all four substituents of the pharmaceutically important spiropyrazolones in moderate to very good yields and in most cases with excellent diastereoselectivities and good to excellent enantioselectivities.

chemistry.chemical_compoundchemistry010405 organic chemistryStereochemistryOrganic ChemistryEnantioselective synthesisPyrazolones010402 general chemistry01 natural sciencesCarbeneCatalysis0104 chemical sciencesCatalysisSynthesis
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