Direct synthesis of alpha-hydroxy acids through selective oxidation of diols mediated by homogeneous and heterogeneous TEMPO (Comunicazione a convegno)

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  • Direct synthesis of alpha-hydroxy acids through selective oxidation of diols mediated by homogeneous and heterogeneous TEMPO (Comunicazione a convegno) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
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  • Maria Luisa Testa, Pamela Gancitano, Rosaria Ciriminna, Mario Pagliaro (2004)
    Direct synthesis of alpha-hydroxy acids through selective oxidation of diols mediated by homogeneous and heterogeneous TEMPO
    in ECSOC-8. 8th International Electronic Conference on Synthetic Organic Chemistry, WEB, 1-30 november 2004
    (literal)
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  • Maria Luisa Testa, Pamela Gancitano, Rosaria Ciriminna, Mario Pagliaro (literal)
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  • Contribute included in SECTION A: GENERAL ORGANIC SYNTHESIS (literal)
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  • http://www.usc.es/congresos/ecsoc/8/conference.htm (literal)
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  • Istituto per lo Studio dei Materiali Nanostrutturati, CNR, Palermo (Italy) (literal)
Titolo
  • Direct synthesis of alpha-hydroxy acids through selective oxidation of diols mediated by homogeneous and heterogeneous TEMPO (literal)
Abstract
  • alpha-Hydroxy acids are pivotal components in a variety of compounds with important biological activity. Here we report an easy strategy which allows to synthesise a-hydroxy acids in a two-step oxidation process, involving first the cis-dihydroxylation of a terminal alkenes (catalyzed by ruthenium) followed by subsequent oxidation with TEMPO either dissolved in the homogeneous phase or entrapped in a sol-gel matrix. This work extends what we recently found concerning the synthesis of amino hydroxy acids by oxidation of the primary hydroxyls in aminodiols. (literal)
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