<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1870-249X</journal-id>
<journal-title><![CDATA[Journal of the Mexican Chemical Society]]></journal-title>
<abbrev-journal-title><![CDATA[J. Mex. Chem. Soc]]></abbrev-journal-title>
<issn>1870-249X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Química de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-249X2006000100008</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Synthesis of Pregnenolone-Pregnenolone Dimer via Ring A-Ring A connection]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Figueroa Valverde]]></surname>
<given-names><![CDATA[Lauro]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Díaz Cedillo]]></surname>
<given-names><![CDATA[Francisco]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tolosa]]></surname>
<given-names><![CDATA[Ligia]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Maldonado]]></surname>
<given-names><![CDATA[Guadalupe]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ceballos Reyes]]></surname>
<given-names><![CDATA[Guillermo]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Autónoma de Campeche  ]]></institution>
<addr-line><![CDATA[Campeche ]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Instituto Politécnico Nacional Escuela Nacional de Ciencias Biológicas ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Instituto Politécnico Nacional Escuela Superior de Medicina ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2006</year>
</pub-date>
<volume>50</volume>
<numero>1</numero>
<fpage>42</fpage>
<lpage>45</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2006000100008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2006000100008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2006000100008&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[A pregnenolone-pregnenolone dimer was synthesized. The route involved preparation of pregnenolone hemisuccinate (2) by the esterification of pregnenolone (1) using succinic anhydride and pyridine, followed by formation of pregnenolone-derivate (3) and preparation of pregnenolone-pregnenolone dimer (4).]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[En este trabajo, fue sintetizado un dímero pregnenolona-pregnenolona. La ruta incluye la preparación del hemisuccinato de pregnenolona (2) por la esterificación de pregnenolona (1) usando anhídrido succínico y piridina, seguido por la formación del derivado de pregnenolona (3) y preparación del dímero pregnenolona-pregnenolona (4).]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Pregnenolone]]></kwd>
<kwd lng="en"><![CDATA[dimer]]></kwd>
<kwd lng="en"><![CDATA[hemisuccinate]]></kwd>
<kwd lng="es"><![CDATA[Pregnenolona]]></kwd>
<kwd lng="es"><![CDATA[dímero]]></kwd>
<kwd lng="es"><![CDATA[hemisuccinato]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Article</font></p>      <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="4"><b>Synthesis of Pregnenolone&#45;Pregnenolone Dimer via Ring A&#45;Ring A connection</b></font></p>  	    <p align="center"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="2"><b>Lauro Figueroa Valverde,*<sup>1</sup> Francisco D&iacute;az Cedillo,<sup>2</sup> Ligia Tolosa,<sup>1</sup> Guadalupe Maldonado,<sup>1</sup> Guillermo Ceballos Reyes<sup>3</sup></b></font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>1</sup> <i>Universidad Aut&oacute;noma de Campeche, Av. Agust&iacute;n Melgar, Col Buenavista C.P.24030 Campeche Campeche, M&eacute;xico.,</i> <i>Telephone: (981)8184246, (981) 8119800 Ext. 73006</i>, e&#45;mail: *<a href="mailto:lauro_1999@yahoo.com">lauro_1999@yahoo.com</a></font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>2</sup> <i>Escuela Nacional de Ciencias Biol&oacute;gicas, Instituto Polit&eacute;cnico Nacional, Col. Santo Tom&aacute;s, M&eacute;xico, D.F., C.P. 11340.</i></font></p>  	    <p align="justify"><font face="verdana" size="2"><sup>3</sup> <i>Escuela Superior de Medicina, Instituto Polit&eacute;cnico Nacional, D&iacute;az Mir&oacute;n esq. Plan de Ayala s/n Col. Plutarco El&iacute;as Calles,</i> <i>M&eacute;xico, D.F., C.P. 11340.</i></font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">Recibido el 24 de enero del 2006.    <br> 	Aceptado el 27 de marzo del 2006.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>  	    <p align="justify"><font face="verdana" size="2">A pregnenolone&#45;pregnenolone dimer was synthesized. The route involved preparation of pregnenolone hemisuccinate <b>(2)</b> by the esterification of pregnenolone <b>(1)</b> using succinic anhydride and pyridine, followed by formation of pregnenolone&#45;derivate <b>(3)</b> and preparation of pregnenolone&#45;pregnenolone dimer <b>(4).</b></font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> Pregnenolone, dimer, hemisuccinate.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>  	    <p align="justify"><font face="verdana" size="2">En este trabajo, fue sintetizado un d&iacute;mero pregnenolona&#45;pregnenolona. La ruta incluye la preparaci&oacute;n del hemisuccinato de pregnenolona <b>(2)</b> por la esterificaci&oacute;n de pregnenolona <b>(1)</b> usando anh&iacute;drido succ&iacute;nico y piridina, seguido por la formaci&oacute;n del derivado de pregnenolona <b>(3)</b> y preparaci&oacute;n del d&iacute;mero pregnenolona&#45;pregnenolona <b>(4).</b></font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Pregnenolona, d&iacute;mero, hemisuccinato.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v50n1/v50n1a8.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>    	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">1.&nbsp;Compagnone, N. A.; Mellon, S. 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