1,720,982 research outputs found

    The preparation of beta-hydroxysulfoxides

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    Oxidation of beta-hydroxy thioethers with MnO2-aqu.35%/HCl in methanol gives beta-hydroxy sulfoxides in high yields

    CARBONYL REGENERATION FROM PARA-TOLUENSULFONHYLHYDRAZONES BY TRIMETHYLCHLOROSILANE-DIMETHYLSULFOXIDE

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    Treatment of p-tosylhydrazones of saturated and alpha,beta-unsaturated ketones and aldehydes with trimethylchlorosilane-dimethyl sulphoxide in dry acetonitrile affords the corresponding carbonyl compounds in excellent yields under mild conditions

    REGIOSPECIFIC CONVERSION OF ALPHA,BETA-EPOXY ACETATES TO 3-CHLORO-2-HYDROXY ACETATES

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    3-chloro-2-hydroxy acetates are easily obtained by treating alpha,beta-epoxy acetates with chlorotrimethylsilane-dimethyl sulphoxide in acetonitrile

    SULFOXIDES FROM THIOETHERS AND MNO2-HCL

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    Treatment of thioethers with manganese(IV)oxide-35% aqueous hydrogen chloride in methanol gives sulfoxides in high yields; sulfones are not produce

    OXIDATION OF ALPHA-ACETOXY ACETALS WITH TRICHLOROISOCYANURIC ACID

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    alpha-Acetoxy acid methyl esters are prepared in excellent yields by treating aliphatic alpha-acetoxy dimethyl acetals with trichloroisocyanuric acid in DMF

    Hg(II)-coordination by sugar-acids: Role of the hydroxy groups

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    A solution study on the ability of some derivatised sugars [glucuronic acid (GluA), galacturonic acid (GalA) and glucosaminic acid (GlNA)] to complex the Hg(II) ion is reported. The stability constants of the complex species were determined by potentiometric measurements while H-1 NMR experiments allow to define the coordination sites of sugar molecules. GluA coordinates the metal ion through the carboxylic oxygen and the O-4 hydroxyl group and is found to form more stable complexes with respect to GalA in which metal ligation is from the carboxylic oxygen and the O-5 ring oxygen. GlNA forms stable complexes chelating Hg(II) ion through carboxylic oxygen and the a-amino group. The ternary 2,2 ́-bipyridine containing systems were also investigated by means of potentiometric studies. The ML2 complexes were also isolated in the solid state and characterised by IR spectroscopy

    REACTIONS OF THE TRIMETHYLCHLOROSILANE-DIMETHYL SULPHOXIDE REAGENT WITH CARBONYL COMPOUNDS

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    The Me3SiCl-Me2SO system is an efficient reagent for the smooth chlorination of unconjugated carbonyl compds. at the more substituted α-carbon atom. β-Dicarbonyl substrates are transformed into α-chloro-α-thiomethyl ether derivs
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