<?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>S1870-249X2017000300167</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Synthesis of (E)-(4-(Aryl)phenyl)(3-(2-(1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl)vinyl)benzofuran-2-yl)methanones by Claisen Schmidt-Suzuki Cross Coupling and their Antibacterial and Antifungal Activity]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ashok]]></surname>
<given-names><![CDATA[Dongamanti]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ziauddin]]></surname>
<given-names><![CDATA[Mohammad]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lakshmi]]></surname>
<given-names><![CDATA[Bommidi Vijaya]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sarasija]]></surname>
<given-names><![CDATA[Madderla]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Osmania University Department of Chemistry Green and Medicinal Chemistry laboratory]]></institution>
<addr-line><![CDATA[Hyderabad ]]></addr-line>
<country>India</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Osmania University University College of technology Department of pharmaceutical Sciences]]></institution>
<addr-line><![CDATA[Hyderabad ]]></addr-line>
<country>India</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2017</year>
</pub-date>
<volume>61</volume>
<numero>3</numero>
<fpage>167</fpage>
<lpage>176</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2017000300167&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2017000300167&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2017000300167&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract. A series of ten novel (E)-(4-(aryl)phenyl)(3-(2-(1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl)vinyl)benzofuran-2-yl)methanones (7a-j) derivatives were prepared by traditional Claisen-Schmidt and Suzuki cross-coupling reaction under conventional and microwave irradiation conditions. The structures of all the newly synthesized compounds were established on the basis of FTIR, 1H NMR, 13C NMR, mass spectral data and elemental analysis. The products were assayed for their in vitro antibacterial activity against different types of bacterial strains. Further the antifungal activity was examined by inhibitory action against three fungal strains such as Aspergillus niger, Aspergillus flavus and Fusarium oxysporum.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen. Una serie de diez nuevos derivados de E)-(4-(aril)fenil)(3-(2-(1-fenil-3-(tiofen-2-il)-1H-pirazol-4-il)vinil)benzofuran-2-il)metanonas (7a-j) se prepararon mediante la reacción tradicional de Claisen-Schmidt y el acoplamiento cruzado de Suzuki bajo condiciones convencionales e irradiacción de microondas. Las estructuras de todos los nuevos compuestos sintetizados fueron establecidas de acuerdo a FTIR, 1H NMR, 13C NMR, espectrometría de masas y analisís elemental. La actividad antibacterial in vitro de los productos fue determinada frente a diferentes tipos de cepas bacterianas. Además, se examinó la actividad antifúngica por acción inhibitoria frente a tres cepas de hongos tales como Aspergillus niger, Aspergillus flavus y Fusarium oxysporum.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Aromatic boronic acid]]></kwd>
<kwd lng="en"><![CDATA[Antimicrobial activity]]></kwd>
<kwd lng="en"><![CDATA[Microwave irradiation]]></kwd>
<kwd lng="en"><![CDATA[Claisen-Schimdt]]></kwd>
<kwd lng="en"><![CDATA[Suzuki cross-coupling reaction]]></kwd>
<kwd lng="es"><![CDATA[Ácido boronico aromático]]></kwd>
<kwd lng="es"><![CDATA[Actividad antimicrobiana]]></kwd>
<kwd lng="es"><![CDATA[Irradiación de microondas]]></kwd>
<kwd lng="es"><![CDATA[Reacción de Claisen-Scmidt]]></kwd>
<kwd lng="es"><![CDATA[Reacción de acoplamiento cruzado de Suzuki]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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