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  <channel rdf:about="http://repositoriodigital.ipn.mx/handle/123456789/2838">
    <title>DSpace Collection:</title>
    <link>http://repositoriodigital.ipn.mx/handle/123456789/2838</link>
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        <rdf:li rdf:resource="http://repositoriodigital.ipn.mx/handle/123456789/12374" />
        <rdf:li rdf:resource="http://repositoriodigital.ipn.mx/handle/123456789/12373" />
        <rdf:li rdf:resource="http://repositoriodigital.ipn.mx/handle/123456789/12372" />
        <rdf:li rdf:resource="http://repositoriodigital.ipn.mx/handle/123456789/12371" />
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    <dc:date>2026-04-22T19:00:01Z</dc:date>
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  <item rdf:about="http://repositoriodigital.ipn.mx/handle/123456789/12374">
    <title>Hypolipidemic Effect of Seed Oil of Noni (Morinda citrifolia)</title>
    <link>http://repositoriodigital.ipn.mx/handle/123456789/12374</link>
    <description>Title: Hypolipidemic Effect of Seed Oil of Noni (Morinda citrifolia)
Authors: Cruz López, María del Carmen
Abstract: Morinda citrifolia, has been reported to posses different biological activities and almost all parts of this have been studied phytochemically.&#xD;
However there are few studies on the seeds of fruit. The objective of present study was investigated the effect to Noni Seed Oil (NSO) on&#xD;
serum lipid levels in normolipidemic and hyperlipidemic induced mice. We find that administration of noni oil causes a reduction in total&#xD;
cholesterol and triglycerides levels in both models. However hypolipidemic effect is higher when hyperlipidemia is presented.
Description: Hypolipidemic Effect of Seed Oil of Noni (Morinda citrifolia)</description>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositoriodigital.ipn.mx/handle/123456789/12373">
    <title>Aryloxyacetic esters structurally related to a-Asarone as potential antifungal agents</title>
    <link>http://repositoriodigital.ipn.mx/handle/123456789/12373</link>
    <description>Title: Aryloxyacetic esters structurally related to a-Asarone as potential antifungal agents
Authors: Cruz López, María del Carmen
Abstract: A series of aryloxyacetic ester analogues 8–13 was synthesized based on the&#xD;
potential pharmacophores of the antifungal agents a-Asarone (1) and 2–5. Their antifungal&#xD;
activity was tested in vitro for their growth inhibitory activities against pathogenic&#xD;
fungi. The in vitro antifungal evaluation of these alkyl and aryl esters shows that&#xD;
derivatives 10 displayed the highest antifungal and fungicidal activities against Cryptococcus&#xD;
neoformans and C. gattii. These results support the idea that the phenoxyacetic&#xD;
frame is a potent pharmacophore for the design of potential antifungal drugs.
Description: Aryloxyacetic esters structurally related to a-Asarone&#xD;
as potential antifungal agents</description>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositoriodigital.ipn.mx/handle/123456789/12372">
    <title>Efficient Synthetic Approach to Substituted Benzo[b]furans and Benzo[b] thiophenes by Iodine-Promoted Cyclization of Enaminones</title>
    <link>http://repositoriodigital.ipn.mx/handle/123456789/12372</link>
    <description>Title: Efficient Synthetic Approach to Substituted Benzo[b]furans and Benzo[b] thiophenes by Iodine-Promoted Cyclization of Enaminones
Authors: Cruz López, María del Carmen
Abstract: An efficient synthetic approach to the substituted benzo[b]furan and benzo[b]thiophene scaffolds by&#xD;
iodine-mediated cyclization of the corresponding enaminones is described. This protocol was applied to a&#xD;
large series of these latter precursors to afford the respective benzoheterocycles substituted at the C-2&#xD;
position by a carbonyl group functionality. A study of the factors that control this process reveals that&#xD;
the reactivity depends on the presence of electron-donor groups in the aryl ring of the aryloxycarbonylic&#xD;
and arylthiocarbonylic moieties.
Description: Efficient Synthetic Approach to Substituted Benzo[b]furans and Benzo[b] thiophenes by Iodine-Promoted Cyclization of Enaminones</description>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositoriodigital.ipn.mx/handle/123456789/12371">
    <title>New Approach for the Construction of the Coumarin Frame and Application in the Total Synthesis of Natural Products</title>
    <link>http://repositoriodigital.ipn.mx/handle/123456789/12371</link>
    <description>Title: New Approach for the Construction of the Coumarin Frame and Application in the Total Synthesis of Natural Products
Authors: Cruz López, María del Carmen
Abstract: A new synthetic approach is described for building the coumarin scaffold through the Lewis acidpromoted&#xD;
cyclization of novel aryl 3-(dimethylamino)prop-2-enoates 2a – 2f. The latter precursors were&#xD;
prepared via aminomethylenation of the corresponding aryl acetates 4a – 4f with the Bredereck reagent.&#xD;
This approach was used for the synthesis of biologically active natural compounds 1a – 1f, through a&#xD;
three-step procedure starting from the corresponding phenols.
Description: New Approach for the Construction of the Coumarin Frame and Application in the Total Synthesis of Natural Products</description>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </item>
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