<?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>S1870-249X2007000400008</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Green Oxidation of Organic Compounds: Manganese Sulphate/Oxone®/Water]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vázquez Sánchez]]></surname>
<given-names><![CDATA[Adrián]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ávila Zárraga]]></surname>
<given-names><![CDATA[José Gustavo]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Nacional Autónoma de México, Facultad de Química ]]></institution>
<addr-line><![CDATA[México Distrito Federal]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2007</year>
</pub-date>
<volume>51</volume>
<numero>4</numero>
<fpage>213</fpage>
<lpage>216</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2007000400008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2007000400008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2007000400008&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[We present a methodology for the oxidation of aromatic organic compounds based on manganese sulphate, Oxone® and water. The proposed method, which involves mild reaction conditions, was shown to produce various functional groups of interest in good yield, when applied to amines, alcohols and benzylic groups. This method has several advantageous characteristics, including low-cost reagents, aqueous reaction conditions, moderate temperatures, and short reaction times.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Presentamos una nueva metodología para la oxidación de compuestos aromáticos basada en sulfato de manganeso, Oxone® y agua. El método propuesto, el cual involucra condiciones de reacción suaves, produce distintos grupos funcionales de interés en buenos rendimientos, cuando se aplica a aminas, alcoholes y metilos bencílicos. Este método tiene varias ventajas, incluyendo bajo costo de reactivos, medio acuoso, temperaturas moderadas y tiempos cortos de reacción.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Green oxidation]]></kwd>
<kwd lng="en"><![CDATA[aromatic compounds]]></kwd>
<kwd lng="en"><![CDATA[managanese sulphate]]></kwd>
<kwd lng="en"><![CDATA[oxone]]></kwd>
<kwd lng="en"><![CDATA[amines]]></kwd>
<kwd lng="en"><![CDATA[alcohols]]></kwd>
<kwd lng="en"><![CDATA[benzylic groups]]></kwd>
<kwd lng="es"><![CDATA[Oxidación verde]]></kwd>
<kwd lng="es"><![CDATA[compuestos aromáticos]]></kwd>
<kwd lng="es"><![CDATA[sulfato de manganeso]]></kwd>
<kwd lng="es"><![CDATA[oxone]]></kwd>
<kwd lng="es"><![CDATA[aminas]]></kwd>
<kwd lng="es"><![CDATA[alcoholes]]></kwd>
<kwd lng="es"><![CDATA[grupos bencílicos]]></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>Green Oxidation of Organic Compounds: Manganese Sulphate/Oxone&reg;/Water</b></font></p>  	    <p align="center"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="2"><b>Adri&aacute;n V&aacute;zquez S&aacute;nchez and Jos&eacute; Gustavo &Aacute;vila Z&aacute;rraga*</b></font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><i>Facultad de Qu&iacute;mica, Universidad Nacional Aut&oacute;noma de M&eacute;xico. Circuito Escolar, Ciudad Universitaria. Coyoac&aacute;n 04510, M&eacute;xico, D. F., M&eacute;xico</i></font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">Recibido el 15 de agosto de 2007    ]]></body>
<body><![CDATA[<br> 	Aceptado el 26 de noviembre de 2007</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">We present a methodology for the oxidation of aromatic organic compounds based on manganese sulphate, Oxone&reg; and water. The proposed method, which involves mild reaction conditions, was shown to produce various functional groups of interest in good yield, when applied to amines, alcohols and benzylic groups. This method has several advantageous characteristics, including low&#45;cost reagents, aqueous reaction conditions, moderate temperatures, and short reaction times.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Key words:</b> Green oxidation, aromatic compounds, managanese sulphate, oxone, amines, alcohols, benzylic groups.</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">Presentamos una nueva metodolog&iacute;a para la oxidaci&oacute;n de compuestos arom&aacute;ticos basada en sulfato de manganeso, Oxone&reg; y agua. El m&eacute;todo propuesto, el cual involucra condiciones de reacci&oacute;n suaves, produce distintos grupos funcionales de inter&eacute;s en buenos rendimientos, cuando se aplica a aminas, alcoholes y metilos benc&iacute;licos. Este m&eacute;todo tiene varias ventajas, incluyendo bajo costo de reactivos, medio acuoso, temperaturas moderadas y tiempos cortos de reacci&oacute;n.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Palabras clave:</b> Oxidaci&oacute;n verde, compuestos arom&aacute;ticos, sulfato de manganeso, oxone, aminas, alcoholes, grupos benc&iacute;licos.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    ]]></body>
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