http://www.cnr.it/ontology/cnr/individuo/prodotto/ID213988
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)
- Alternative label
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
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- Maria Luisa Testa, Pamela Gancitano, Rosaria Ciriminna, Mario Pagliaro (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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