<?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>S1870-249X2005000400005</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Kinetic Aspects of Soai's Asymmetric Autocatalysis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Thomas]]></surname>
<given-names><![CDATA[Buhse]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Autónoma del Estado de Morelos Centro de Investigaciones Químicas ]]></institution>
<addr-line><![CDATA[Cuernavaca Morelos]]></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>4</numero>
<fpage>328</fpage>
<lpage>335</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2005000400005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2005000400005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2005000400005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Recent kinetic studies are discussed that shed light on the reaction mechanism of the autocatalytic addition of diisopropylzinc to pyrimidine carbaldehydes (Soai reaction). Soai's reaction stands for the exclusive example of chirally autocatalytic reaction system in organic chemistry and has attracted close attention from several viewpoints: as possible account for the origin of biomolecular homochirality, as potential innovation in enantioselective synthesis or as a further remarkable manifestation of nonlinear dynamics in chemical systems. It is indicated that the reaction is driven by enantioselective autocatalysis and mutual inhibition as the essential components. A numerical approach reveals that experimentally observed chiral amplification and mirror-symmetry breaking can be readily reproduced by a comparatively simple kinetic model that considers monomers as the catalytic species.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Se discuten estudios cinéticos recientes que dan luz sobre el mecanismo de reacción de la adición autocatalítica de diisopropilzinc en pirimidilcarbaldehídos (reacción de Soai). La reacción de Soai se mantiene como un ejemplo exclusivo de un sistema de reacción quiralmente autocatalítico en química orgánica y que ha atraído la atención desde diversos puntos de vista: como una explicación para el origen de la homoquiralidad biomolecular, como innovación potencial en la síntesis enantioselectiva o como una notable manifestación de la dinámica no lineal en sistemas químicos. Se ha mostrado que la reacción es dirigida por autocatálisis enantioselectiva e inhibición mutua como procesos esenciales. Una aproximación numérica revela que la amplificación quiral observada experimentalmente y el rompimiento de la simetría especular pueden ser reproducidas a partir de un modelo cinético comparativamente simple y que considera monómeros como las especies catalíticas.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Soai reaction]]></kwd>
<kwd lng="en"><![CDATA[asymmetric autocatalysis enantioselection]]></kwd>
<kwd lng="es"><![CDATA[Reacción de Soai]]></kwd>
<kwd lng="es"><![CDATA[autocatálisis asimétrica enantioselección]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Article </font></p>  	    <p align="justify">&nbsp;</p>  	    <p align="center"><font face="verdana" size="4"><b>Kinetic Aspects of Soai's Asymmetric Autocatalysis</b></font></p>     <p align="center">&nbsp;</p>  	    <p align="center"><b><font face="verdana" size="2">Thomas Buhse*</font></b></p>     <p align="center">&nbsp;</p>      <p align="justify"><font face="verdana" size="2"><i>Centro de Investigaciones Qu&iacute;micas, Universidad Aut&oacute;noma del Estado de Morelos, Avenida Universidad 1001, Colonia Chamilpa, Cuernavaca 62209, Morelos, M&eacute;xico. Tel/Fax: +52&#45;7773297997, </i>e&#45;mail: <a href="mailto:buhse@uaem.mx" target="_blank">buhse@uaem.mx</a>.</font></p>     <p align="justify">&nbsp;</p>      <p align="justify"><font face="verdana" size="2">Recibido el 18 de octubre del 2005.     ]]></body>
<body><![CDATA[<br>   Aceptado el 21 de noviembre del 2005.</font></p>     <p align="justify">&nbsp;</p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2"> Recent kinetic studies are discussed that shed light on the reaction mechanism of the autocatalytic addition of diisopropylzinc to pyrimidine carbaldehydes (Soai reaction). Soai's reaction stands for the exclusive example of chirally autocatalytic reaction system in organic chemistry and has attracted close attention from several viewpoints: as possible account for the origin of biomolecular homochirality, as potential innovation in enantioselective synthesis or as a further remarkable manifestation of nonlinear dynamics in chemical systems. It is indicated that the reaction is driven by enantioselective autocatalysis and mutual inhibition as the essential components. A numerical approach reveals that experimentally observed chiral amplification and mirror&#45;symmetry breaking can be readily reproduced by a comparatively simple kinetic model that considers monomers as the catalytic species.</font></p>      <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> Soai reaction, asymmetric autocatalysis enantioselection.</font></p> 	    <p align="justify">&nbsp;</p>      <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2"> Se discuten estudios cin&eacute;ticos recientes que dan luz sobre el mecanismo de reacci&oacute;n de la adici&oacute;n autocatal&iacute;tica de diisopropilzinc en pirimidilcarbaldeh&iacute;dos (reacci&oacute;n de Soai). La reacci&oacute;n de Soai se mantiene como un ejemplo exclusivo de un sistema de reacci&oacute;n quiralmente autocatal&iacute;tico en qu&iacute;mica org&aacute;nica y que ha atra&iacute;do la atenci&oacute;n desde diversos puntos de vista: como una explicaci&oacute;n para el origen de la homoquiralidad biomolecular, como innovaci&oacute;n potencial en la s&iacute;ntesis enantioselectiva o como una notable manifestaci&oacute;n de la din&aacute;mica no lineal en sistemas qu&iacute;micos. Se ha mostrado que la reacci&oacute;n es dirigida por autocat&aacute;lisis enantioselectiva e inhibici&oacute;n mutua como procesos esenciales. Una aproximaci&oacute;n num&eacute;rica revela que la amplificaci&oacute;n quiral observada experimentalmente y el rompimiento de la simetr&iacute;a especular pueden ser reproducidas a partir de un modelo cin&eacute;tico comparativamente simple y que considera mon&oacute;meros como las especies catal&iacute;ticas.</font></p>      <p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Reacci&oacute;n de Soai, autocat&aacute;lisis asim&eacute;trica enantioselecci&oacute;n.</font></p> 	    <p align="justify">&nbsp;</p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><a href="../pdf/jmcs/v49n4/v49n4a5.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p> 	    <p align="justify">&nbsp;</p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgements</b></font></p>  	    <p align="justify"><font face="verdana" size="2">The author thanks the following collaborators and students who contributed to the present work: Jean&#45;Claude Micheau, Dominique Lavabre, Jean&#45;Michel Grevy, Ram&oacute;n Hern&aacute;ndez Lamoneda as well as Jes&uacute;s Rivera Islas and Hayd&eacute;e Rojas Cabrera. Also financial support from CONACYT research grant 34236&#45;E is gratefully acknowledged.</font></p> 	    <p align="justify">&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.&nbsp;Soai, K.; Shibata, T.; Morioka, H.; Choji, K. <i>Nature</i> <b>1995</b>, <i>378,</i> 767&#45;768;    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4892581&pid=S1870-249X200500040000500001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> Soai, K.; Shibata, T. In: <i>Advances in BioChirality;</i> P&aacute;lyi, G.; Zucchi, C.; Caglioti; L. (Eds.) 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