<?xml version="1.0" encoding="UTF-8"?>
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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://repositoriodigital.ipn.mx/handle/123456789/2838" />
  <subtitle />
  <id>http://repositoriodigital.ipn.mx/handle/123456789/2838</id>
  <updated>2026-04-22T19:00:01Z</updated>
  <dc:date>2026-04-22T19:00:01Z</dc:date>
  <entry>
    <title>Hypolipidemic Effect of Seed Oil of Noni (Morinda citrifolia)</title>
    <link rel="alternate" href="http://repositoriodigital.ipn.mx/handle/123456789/12374" />
    <author>
      <name>Cruz López, María del Carmen</name>
    </author>
    <id>http://repositoriodigital.ipn.mx/handle/123456789/12374</id>
    <updated>2019-10-02T17:15:20Z</updated>
    <published>2013-01-30T00:00:00Z</published>
    <summary type="text">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)</summary>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Aryloxyacetic esters structurally related to a-Asarone as potential antifungal agents</title>
    <link rel="alternate" href="http://repositoriodigital.ipn.mx/handle/123456789/12373" />
    <author>
      <name>Cruz López, María del Carmen</name>
    </author>
    <id>http://repositoriodigital.ipn.mx/handle/123456789/12373</id>
    <updated>2019-10-02T17:17:39Z</updated>
    <published>2013-01-30T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Efficient Synthetic Approach to Substituted Benzo[b]furans and Benzo[b] thiophenes by Iodine-Promoted Cyclization of Enaminones</title>
    <link rel="alternate" href="http://repositoriodigital.ipn.mx/handle/123456789/12372" />
    <author>
      <name>Cruz López, María del Carmen</name>
    </author>
    <id>http://repositoriodigital.ipn.mx/handle/123456789/12372</id>
    <updated>2019-10-02T17:17:34Z</updated>
    <published>2013-01-30T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>New Approach for the Construction of the Coumarin Frame and Application in the Total Synthesis of Natural Products</title>
    <link rel="alternate" href="http://repositoriodigital.ipn.mx/handle/123456789/12371" />
    <author>
      <name>Cruz López, María del Carmen</name>
    </author>
    <id>http://repositoriodigital.ipn.mx/handle/123456789/12371</id>
    <updated>2019-10-02T17:15:17Z</updated>
    <published>2013-01-30T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>2013-01-30T00:00:00Z</dc:date>
  </entry>
</feed>

