47 research outputs found

    A Selective, Efficient and Environmentally Friendly Method for the Oxidative Cleavage of Glycols

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    A catalytic methodology for the oxidative cleavage of vicinal diols is described as an advantageous alternative in terms of the environmental impact on classical methods involving toxic oxidants. The novel strategy is based on the use of dioxomolybdenum(VI) complexes as catalysts and dimethyl sulfoxide (DMSO) as an oxidant and displays high selectivity and a broad scope for glycol cleavage. In addition, the developed system is also useful for the oxidation of acyloins to diketones.Ministerio de Economía y Competitividad (MINECO) and FEDER (CTQ2013-48937-C2-1-P) and Junta de Castilla y León (BU237U13

    A short and enantioselective synthesis of (<i>S</i>)-<i>N</i>-tosyl-l-naphthylglycine

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    291-293Synthesis of (S)-N-tosyl-1-naphthylglycine with good optical purity was achieved using Sharpless asymmetric aminohydroxylation as key step

    Cu-exchanged Y-zeolite: A heterogeneous catalyst for the synthesis of α-aminoketones

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    515-517Cu-zeolite catalyzes the amination of silyl enol ethers using PhI= NTs producing α-amino ketones in good yields

    Synthesis Of Some Hydroxymethylbromo-Phenols Of Marine Origin

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    Enantioselective synthesis of (<i style="">S</i>)-<i style=""><img src='/image/spc_char/alpha.gif' border=0></i>-arylpropionic acids <i style="">via</i> Pd-catalyzed kinetic resolution of benzylic alcohols

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    557-562A convenient synthetic route for the synthesis of three (S)-a-propionic acids, (S)-naproxen (90% ee), (S)-ibuprofen (82% ee) and (S)-phenylpropionic acid (92% ee) is described. Pd-catalyzed oxidative kinetic resolution of the corresponding benzylic alcohols is used as a key step to introduce stereogenicity into the molecule

    Neodymium acetylacetonate. A new heterogeneous catalyst for transfer hydrogenation of carbonyl compounds

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    409-410Neodymium acetylacetonate, Nd (acac)3 3H2O, has been found to exhibit high activity towards the transfer hydrogenation of carbonyl compounds using 2-propanol as hydrogen source under truly heterogeneous phase to afford the corresponding alcohols in 63-81% yield
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