<?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>S1870-249X2022000400421</article-id>
<article-id pub-id-type="doi">10.29356/jmcs.v66i4.1718</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Six-Membered Heterocyclic Boronate Esters. Synthesis and Structural Analysis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[León-Negrete]]></surname>
<given-names><![CDATA[Ariana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Villamil-Ramos]]></surname>
<given-names><![CDATA[Raúl]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez-Portillo]]></surname>
<given-names><![CDATA[Paola]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[González-Hernández]]></surname>
<given-names><![CDATA[Arturo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Barba]]></surname>
<given-names><![CDATA[Victor]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<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>12</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2022</year>
</pub-date>
<volume>66</volume>
<numero>4</numero>
<fpage>421</fpage>
<lpage>432</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2022000400421&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2022000400421&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2022000400421&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Nine heterocyclic zwitterionic boronate esters derived from carbonylphenylboronic acids and amino-diols are described. Compounds were prepared by direct condensation reaction between 3- or 4-formyl/acetylphenylboronic acids with 2-amino-2-methyl-1,3-propanediol (1a-1d) or serinol (2-amino-1,3-propanediol) (1e-1h). Compound 2e was obtained by reaction between 4-formylphenylboronic acid and serinol using a solvent mixture methanol/acetone, an aldol condensation reaction was observed. All compounds were characterized by common spectroscopic techniques such as FT-IR, mass spectrometry, and multinuclear 1H, 13C and 11B NMR spectroscopy. 11B NMR spectra showed signals between &#948; = 1.9 to 7.3 ppm for all compounds, indicating a tetracoordinated environment for the boron atoms in solution. X-ray diffraction analysis showed that boronates are contained in six-membered heterocycles, which have a chair conformation with -OH and -NH3 + substituents in syn disposition. The formation of channels in the crystal lattice that are filled with water and supported by hydrogen bonding interactions is noteworthy.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen En el presente trabajo se describen nueve ésteres de boro zwitteriónicos, derivados de ácidos cabonilfenilborónicos. Los compuestos fueron obtenidos mediante reacciones de condensación entre el ácido 3- o 4- formil/acetilfenilborónico con 2-amino-2-metil propanodiol (1a-1d) o serinol (1e-1h). El compuesto 2e se sintetizó a través del ácido 4-formilfenilborónico y serinol (2-amino-1,3-propanodiol) utilizando una mezcla de disolventes metanol/acetona, dando lugar a una reacción de condensación aldólica. Los compuestos fueron caracterizados por técnicas espectroscópicas como son FT-IR, espectrometría de masas y espectroscopia multinuclear de RMN 1H, 13C y 11B. El espectro RMN de 11B mostró señales anchas entre &#948; = 1.9 y 7.3 ppm para todos los compuestos, lo cual indica la presencia de átomos de boro tetracoordinados en solución. El análisis por difracción de rayos-X de monocristal mostró la formación de heterociclos de 6 miembros en conformación silla, con una marcada estereoselectividad en donde los grupos -OH y -NH3 + se encuentran en disposición syn. En la red cristalina, se observaron canales ocupados por moléculas de agua y soportados por enlaces de hidrógeno.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Arylboronic acids]]></kwd>
<kwd lng="en"><![CDATA[zwitterionic species]]></kwd>
<kwd lng="en"><![CDATA[boronate esters]]></kwd>
<kwd lng="en"><![CDATA[hydrogen bonds]]></kwd>
<kwd lng="en"><![CDATA[crystallographic analysis]]></kwd>
<kwd lng="es"><![CDATA[Ácidos arilborónicos]]></kwd>
<kwd lng="es"><![CDATA[especies switteriónicas]]></kwd>
<kwd lng="es"><![CDATA[ésteres de boro]]></kwd>
<kwd lng="es"><![CDATA[enlaces de hidrógeno]]></kwd>
<kwd lng="es"><![CDATA[análisis cristalográfico]]></kwd>
</kwd-group>
</article-meta>
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