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  <title>Unitus DSpace</title>
  <link rel="alternate" href="http://http://dspace.unitus.it:80" />
  <subtitle>The DSpace digital repository system captures, stores, indexes, preserves, and distributes digital research material.</subtitle>
  <id>http://http://dspace.unitus.it:80</id>
  <updated>2013-05-21T13:22:09Z</updated>
  <dc:date>2013-05-21T13:22:09Z</dc:date>
  <entry>
    <title>Chemoselective and efficient carboxymethylation of the alcoholic chain of phenols by dimethyl carbonate (DMC).</title>
    <link rel="alternate" href="http://hdl.handle.net/2067/1881" />
    <author>
      <name>Bernini, Roberta</name>
    </author>
    <author>
      <name>Mincione, Enrico</name>
    </author>
    <author>
      <name>Crisante, Fernanda</name>
    </author>
    <author>
      <name>Barontini, Maurizio</name>
    </author>
    <author>
      <name>Fabrizi, Giancarlo</name>
    </author>
    <author>
      <name>Gentili, Patrizia</name>
    </author>
    <id>http://hdl.handle.net/2067/1881</id>
    <updated>2011-06-28T13:21:08Z</updated>
    <published>2006-12-31T23:00:00Z</published>
    <summary type="text">Title: Chemoselective and efficient carboxymethylation of the alcoholic chain of phenols by dimethyl carbonate (DMC).
Authors: Bernini, Roberta; Mincione, Enrico; Crisante, Fernanda; Barontini, Maurizio; Fabrizi, Giancarlo; Gentili, Patrizia
Abstract: The efficiency of dimethyl carbonate (DMC) as chemoselective carbomethoxylating agent of the alcoholic chain of phenols has been investigated. In the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or sulfuric acid as catalysts. New carbomethoxylated phenolic compounds were obtained in quantitative yields. A new efficient derivatization of the aliphatic alcoholic chain of the precious natural hydroxytyrosol is described, which increases the lipophilicity of the hydroxytyrosol. The antioxidant activity of this new carboxymethylated hydroxytyrosol 8 has been investigated using DPPH radical scavenging test. The results showed that this new compound has an antioxidant activity similar to hydroxytyrosol.
Description: L'articolo è disponibile sul sito dell'editore:&#xD;
http://www.sciencedirect.com</summary>
    <dc:date>2006-12-31T23:00:00Z</dc:date>
  </entry>
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