Search results for "carbon"

showing 10 items of 6057 documents

Palladium-Catalyzed Suzuki Carbonylative Reaction of α-Halomethyl Oxime Ethers: A Regioselective Route to Unsymmetrical 1,3-Oxyiminoketones

2014

chemistry.chemical_compoundReaction mechanismchemistryRegioselectivitychemistry.chemical_elementOrganic chemistryGeneral ChemistryOximeCarbonylationPalladiumCatalysisAdvanced Synthesis & Catalysis
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13C NMR Spectral Characterization of 4-Aryl-Substituted Bispyrazolo[3,4-b;4′,3′-e]pyridines

1996

chemistry.chemical_compoundStereochemistryChemistryArylGeneral Materials ScienceGeneral ChemistryCarbon-13 NMRCharacterization (materials science)Magnetic Resonance in Chemistry
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Diastereoselectivity in Organometallic Additions to the Carbonyl Group of Protected Erythrulose Derivatives

1998

We have investigated a number of nucleophillic additions to L-erythrulose derivatives (4-12) bearing protective O-silyl, O-benzyl, and O-trityl groups in various relative positions. The results are discussed in the frame of chelated vs nonchelated transition states with additional support of previously published theoretical calculations. Sound evidence appears to exist for the formation of alpha-chelates as the key intermediates in nucleophillic additions to these alpha,beta-dioxygenated ketones. Since such evidence is still lacking in the case of beta-chelates, proposals of their intermediacy have been relegated in favor of the more solid Felkin-Anh model, which predicts the same stereoche…

chemistry.chemical_compoundStereochemistryChemistryOrganic ChemistryErythruloseCarbonyl groupTransition stateThe Journal of Organic Chemistry
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CO2 as a C1-Building Block for Dialkyl Carbonate Synthesis

2002

Carbon dioxide, one of the major man-made greenhouse gas, is a renewable resource of carbon which can be viewed as a C1 synthon to build valuable chemicals. The development of new applications is of major interest considering CO2 conversion and environmentally friendly reactions. As chemical catalysis offers interesting options, we are studying the molecular design of catalysts for the formation of dialkyl carbonates from alcohols and CO2. This paper reports results on the mechanistic approach for dialkyl carbonate formation with alkoxybutyl tin(IV) compounds. The insertion of CO2 into Sn-OR bonds (R = Me, 1Pr) occurs at atmospheric pressure and room temperature leading to alkylcarbonato ti…

chemistry.chemical_compoundSupercritical carbon dioxidechemistrySynthonCarbon dioxideCarbonatechemistry.chemical_elementOrganic chemistryDimethyl carbonateTinSupercritical fluidCatalysis
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ChemInform Abstract: Baeyer-Villiger Oxidation of Ketones with a Silica-Supported Peracid in Supercritical Carbon Dioxide under Flow Conditions.

2009

[2-Percarboxyethyl]-functionalized silica reacts with ketones in supercritical carbon dioxide at 250 bar and 40 °C under flow conditions to yield the corresponding esters and lactones. The solid reagent can be easily recycled through treatment with 70% hydrogen peroxide in the presence of an acid at 0 °C. This procedure not only simplifies the isolation of the reaction products, but has the advantage of using only water and carbon dioxide as solvents under mild conditions.

chemistry.chemical_compoundSupercritical carbon dioxidechemistryYield (chemistry)ReagentCarbon dioxideOrganic chemistryDehydrogenationGeneral MedicineHydrogen peroxideBaeyer–Villiger oxidationBar (unit)ChemInform
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Phase Equilibria Involved in the Extractive Distillation of Cyclohexane + Cyclohexene Using Diethyl Carbonate as an Entrainer

2011

Isobaric vapor–liquid equilibrium (VLE) data at 100 kPa have been measured for the ternary system cyclohexane + cyclohexene + diethyl carbonate and two constituent binary systems: cyclohexane + diethyl carbonate and cyclohexene + diethyl carbonate. Both binary systems show moderate positive deviations from ideal behavior and do not present an azeotrope. The VLE data have been correlated by the Wilson, universal quasichemical activity coefficient (UNIQUAC), and nonrandom two-liquid (NRTL) equations. The ternary system does not present an azeotrope and is well-estimated from binary interaction parameters. A prediction with the universal functional activity coefficient (UNIFAC)-Dortmund method…

chemistry.chemical_compoundUNIQUACTernary numeral systemChemistryGeneral Chemical EngineeringAzeotropeCyclohexeneDiethyl carbonateNon-random two-liquid modelExtractive distillationThermodynamicsGeneral ChemistryUNIFACJournal of Chemical & Engineering Data
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Recycling and fluxes of carbon gases in a stratified boreal lake following experimental carbon addition

2014

Partly anoxic stratified humic lakes are important sources of methane (CH4) and carbon dioxide (CO2) to the atmosphere. We followed the fate of CH4 and CO2 in a small boreal stratified lake, Alinen Mustajärvi, during 2007–2009. In 2008 and 2009 the lake received additions of dissolved organic carbon (DOC) with stable carbon isotope ratio (δ13C) around 16‰ higher than that of local allochthonous DOC. Carbon transformations in the water column were studied by measurements of δ13C of CH4 and of the dissolved inorganic carbon (DIC). Furthermore, CH4 and CO2 production, consumption and emissions were estimated. Methane oxidation was estimated by a diffusion gradient method. The amount, lo…

chemistry.chemical_compoundWater columnchemistryEcologyEpilimnionEnvironmental chemistryCarbon dioxideDissolved organic carbonAnaerobic oxidation of methanechemistry.chemical_elementCarbonAnoxic watersMethane
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ChemInform Abstract: Palladium-Catalyzed Alkoxy- and Aminocarbonylation of α-Halomethyl Oxime Ethers: Synthesis of 1,3-Alkoxyimino Esters and 1,3-Alk…

2015

The three component reactions of α-bromomethyl oxime ethers, carbon monoxide, and alcohols or aromatic amines give imino esters and amides, respectively.

chemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistrychemistry.chemical_elementheterocyclic compoundsGeneral MedicineOximeCarbonylationCatalysisCarbon monoxidePalladiumChemInform
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Synthesis and structural characterization of cis- and trans-fused 4a,5,6,7,8,8a-hexahydro-2H,4H-1,3-benzodithiines and their 2-methyl and 2,2-dimethy…

2002

Both cis- and trans-fused 4a,5,6,7,8,8a-hexahydro-2H,4H-1,3-benzodithiine together with their 2-methyl and 2,2-dimethyl derivatives were prepared as racemates from the appropriate dithiols obtained via multistep syntheses. The products were characterized by 1 H and 13 C NMR, mass spectrometry, and for two of the cis-fused compounds by X-ray diffraction. 1 H, 1 H vicinal coupling constants indicated that all compounds attain chair-chair conformations as their predominant conformations. All three trans-fused isomers exist in totally biased chair-chair conformations and are essentially conformationally locked, whereas the cis-fused compounds are conformationally mobile and can potentially atta…

chemistry.chemical_compoundchemistryBicyclic moleculeStereochemistryOrganic ChemistryX-ray crystallographyDithiolMoleculeCarbon-13 NMRChemical synthesisConformational isomerismCis–trans isomerismThe Journal of organic chemistry
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Synthesis of Linear and Cyclic Carbonates

2010

chemistry.chemical_compoundchemistryCarbon dioxideOrganic chemistry
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