<?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>S1870-249X2005000200010</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[A Convenient Procedure for the Synthesis of 3&#946;-Hydroxy-6-oxo-5&#945;-steroids: Application to the Synthesis of Laxogenin]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Iglesias-Arteaga]]></surname>
<given-names><![CDATA[Martín A.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Símuta-Lopez]]></surname>
<given-names><![CDATA[Eva M.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Xochihua-Moreno]]></surname>
<given-names><![CDATA[Sergio]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Viñas-Bravo]]></surname>
<given-names><![CDATA[Omar]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Montiel Smith]]></surname>
<given-names><![CDATA[Sara]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Meza Reyes]]></surname>
<given-names><![CDATA[Socorro]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sandoval-Ramírez]]></surname>
<given-names><![CDATA[Jesús]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Nacional Autónoma de México Facultad de Química Departamento de Química Orgánica]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Benemérita Universidad Autónoma de Puebla Facultad de Ciencias Químicas ]]></institution>
<addr-line><![CDATA[Puebla ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<volume>49</volume>
<numero>2</numero>
<fpage>134</fpage>
<lpage>142</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2005000200010&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2005000200010&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2005000200010&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[A convenient pathway to obtain 3&#946;-hydroxy-6-oxo-5&#945;-steroids from 3&#946;-acetoxy &#916;5-steroids is reported; the methodology was applied to the synthesis of laxogenin (7), substance that behaves as a plant growth hormone. This is an alternative way to produce an important functionality found in many examples of naturally occurring steroids. The developed procedure uses inexpensive reagents and can be carried out in four steps. The oxidizing and acidic steps used in this methodology did not affect the labile spiroketal side chain present in diosgenin (16).]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Uma rota conveniente para a síntese de 3&#946;-hidroxi-6-oxo-5&#945;-esteroides a partir de &#916;5-esteroides é descrita tendo sido aplicada para a síntese da laxogenina, substância que apresenta atividade como hormônio de crescimento vegetal. O método é uma alternativa para instalar este grupo funcional importante encontrado em esteróides naturais. O processo descrito utiliza reagentes baratos e pode ser executado em quatro etapas. As etapas de oxidação e de tratamento ácido não afetam a cadeia lateral espirocetálica presente na diosgenina (16).]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[laxogenin]]></kwd>
<kwd lng="en"><![CDATA[diastereoselective epoxidation]]></kwd>
<kwd lng="en"><![CDATA[3&#946;-hydroxy-6-oxo-5&#945;-steroids]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Article</font></p>  	    <p>&nbsp;</p>  	    <p align="center"><font face="verdana" size="4"><b>A Convenient Procedure for the Synthesis of 3&#946;&#45;Hydroxy&#45;6&#45;oxo&#45;5&#945;&#45;steroids. Application to the Synthesis of Laxogenin</b></font></p>      <p>&nbsp;</p>  	    <p align="center"><font face="verdana" size="2"><b>Mart&iacute;n A. Iglesias&#45;Arteaga*<sup>,a</sup>, Eva M. S&iacute;muta&#45;Lopez<sup>b</sup>, Sergio Xochihua&#45;Moreno<sup>b</sup>, Omar Vi&ntilde;as&#45;Bravo<sup>b</sup>, Sara Montiel Smith<sup>b</sup> , Socorro Meza Reyes<sup>b</sup> and Jes&uacute;s Sandoval&#45;Ram&iacute;rez*<sup>,b</sup></b></font></p>  	    <p>&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><i><sup>a</sup> Departamento de Qu&iacute;mica Org&aacute;nica, Facultad de Qu&iacute;mica, Universidad Nacional Aut&oacute;noma de M&eacute;xico,</i> <i>Ciudad Universitaria, 04510 M&eacute;xico &#45; D. F., M&eacute;xico</i>. * e&#45;mail: <a href="mailto:martin.iglesias@servidor.unam.mx">martin.iglesias@servidor.unam.mx</a>.</font></p>      <p align="justify"><font face="verdana" size="2"><i><sup>b</sup> Facultad de Ciencias Qu&iacute;micas, Benem&eacute;rita Universidad Aut&oacute;noma de Puebla, Ciudad Universitaria,</i> <i>72570 Puebla &#45; Pue., M&eacute;xico.</i> *e&#45;mail: <a href="mailto:jsandova@siu.buap.mx">jsandova@siu.buap.mx</a>.</font></p>      <p>&nbsp;</p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Received: June 24, 2004    <br> 	Published on the web: March 30, 2005</font></p>  	    <p>&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>  	    <p align="justify"><font face="verdana" size="2">A convenient pathway to obtain 3&#946;&#45;hydroxy&#45;6&#45;oxo&#45;5&#945;&#45;steroids from 3&#946;&#45;acetoxy &#916;<sup>5</sup>&#45;steroids is reported; the methodology was applied to the synthesis of laxogenin (7), substance that behaves as a plant growth hormone. This is an alternative way to produce an important functionality found in many examples of naturally occurring steroids. The developed procedure uses inexpensive reagents and can be carried out in four steps. The oxidizing and acidic steps used in this methodology did not affect the labile spiroketal side chain present in diosgenin (16).</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> laxogenin, diastereoselective epoxidation, 3&#946;&#45;hydroxy&#45;6&#45;oxo&#45;5&#945;&#45;steroids</font></p>  	    <p>&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>Resumo</b></font></p>  	    <p align="justify"><font face="verdana" size="2">Uma rota conveniente para a s&iacute;ntese de 3&#946;&#45;hidroxi&#45;6&#45;oxo&#45;5&#945;&#45;esteroides a partir de &#916;<sup>5</sup>&#45;esteroides &eacute; descrita tendo sido aplicada para a s&iacute;ntese da laxogenina, subst&acirc;ncia que apresenta atividade como horm&ocirc;nio de crescimento vegetal. O m&eacute;todo &eacute; uma alternativa para instalar este grupo funcional importante encontrado em ester&oacute;ides naturais. O processo descrito utiliza reagentes baratos e pode ser executado em quatro etapas. As etapas de oxida&ccedil;&atilde;o e de tratamento &aacute;cido n&atilde;o afetam a cadeia lateral espirocet&aacute;lica presente na diosgenina (16).</font></p>  	    <p>&nbsp;</p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v49n2/v49n2a10.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>  	    <p>&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>Acknowledgments</b></font></p>  	    <p align="justify"><font face="verdana" size="2">We are indebted to CONACyT, Mexico, for financial support via grant 35235&#45;E and the scholarships granted to S.X.M and O.V.B. We also want to acknowledge Professor Benjam&iacute;n Ruiz for laboratory facilities at the Facultad de Qu&iacute;mica of UNAM.</font></p>  	    <p>&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">1. Hill, R. A.; Makin, H. L. J.; Kirk, D. N.; Murphy, G. M., eds.; <i>Dictionary of Steroids,</i> Chapman and Hall: London, 1991.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4917848&pid=S1870-249X200500020001000001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">2. Adam, G.; Marquardt, V.; <i>Phytochemistry</i> 1986, 25, 1787.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4917850&pid=S1870-249X200500020001000002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	    ]]></body>
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