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&lt;p&gt;&amp;nbsp;&lt;/p&gt;</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Microwave-assisted solid-phase synthesis of the 2,4-disubstituted thiazole 3 on Merrifield Resin is described. The hydroxyl moiety was converted to amine in five steps &amp;ndash; including coupling and cleavage &amp;ndash; within a total reaction time of 2 hours and 26% overall yield. The entire solid-phase synthesis was efficiently monitored by FT-IR/KBr pellets and allows potential use in combinatorial chemistry.</text>
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                <text>New 1,8-dioxooctahydroxanthenes with substituents in the 2-, 3-, and 9-positions were obtained by cyclization with iodine from tandem Michael/Michael adducts. The X-ray molecular structure of the methyl 2-(1,8-dioxo-2,3,4,5,6,7,8,9-octahydro- 1H-xanthen-9-yl)acetate (3a) was solved and shows Introduction Compounds 2a&amp;ndash;d were recently obtained by our research group as products of tandem Michael/Michael additions Scheme 1. Synthesis of octahydroxanthenes 3a&amp;ndash;f by sequential tandem Michael&amp;ndash;iodine-catalyzed cyclization. Reaction conditions: �&amp;ndash;C(O)R5, l-proline, DMSO, room temp., 3 d; then I2 cat., room temp., 5 h.</text>
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                <text>&lt;strong&gt;Luna, Liliana E.&lt;/strong&gt;</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
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                <text>The synthesis of 3-hydroxy-2-hexanone and 2,3-hexanediol, two components of the aggregation pheromone of several cerambycid species, is disclosed in here. Starting from 2-hexanone, through an &amp;alpha;-hydroxylation using (diacetoxyiodo)benzene, 3-hydroxy-2-hexanone is obtained in good yield. Further reduction of this compound, gives 2,3-hexanediol in excellent yield. A study of the &amp;alpha;-hydroxylation reaction of several alkylketones using an hypervalent iodine reagent is also disclosed in here. The synthesis of optically active compounds (R)- and (S)-3-hydroxy-2-hexanone was achieved starting from 2-hexanone with nitrosobenzene and l- and d-proline respectively, in several reaction media.</text>
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                <text>Tetrahedron Letters&amp;nbsp; v. 58, 2017. -- p. 1738-1741</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Cationic latex particles with surface amino groups were prepared by a multistep batch emulsion polymerization. In the first one or two steps, monodisperse cationic latex particles to be used as the seed were synthesized, and in the third step, two different amino-functionalized monomers [aminoethylmethacrylate hydrochloride (AEMH) and vinylbenzylamine hydrochloride (VBAH)] were used to synthesize the final functionalized latex particles. 2,2&amp;prime;-Azobisisobutyramidine dihydrochloride was used as the initiator, and different concentrations of two quaternary ammonium emulsifiers with hydrophobic chains of different lengths were examined. To characterize the final latexes yields were obtained gravimetrically, and particle size distributions and average particle diameters were determined by transmission electron microscopy and photon correlation spectroscopy. The amount of amino groups was determined by fluorimetry. The effect of the amino-functional monomer used on the final latexes and the colloidal behavior of the system were studied. The influence of the different conditions utilized to synthesize the latexes on the colloidal stability of the particles was evaluated in terms of the Fuchs stability ratio and electrophoretic mobility. High yields of the amino-functional monomers were obtained. Surface amino, amidine, and quaternary ammonium groups provided the cationic character. The colloidal stability behavior of the products obtained was compatible with their cationic character.</text>
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                <text>1,4-Thiazepines derivatives are pharmacologically important heterocycles with different applications in medicinal chemistry. In the present work, we describe the preparation of new bicyclic thiazolidinyl-1,4-thiazepines 3 by reaction between azadithiane compounds and Michael acceptors. The reaction scope was explored and the yields were optimized. The activity of the new compounds was evaluated against Nippostrongylus brasiliensis and Caenorhabditis elegans as anthelmintic models and Trypanosoma brucei brucei. The most active compound was 3l, showing an EC50 = 2.8 &amp;plusmn; 0.7 &amp;mu;M against T. b. brucei and a selectivity index &amp;gt;71.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis of bimetallic trifluoroacetates through a crystallochemical investigation of their monometallic counterparts : |b the case of (A, A&amp;rsquo;) (CF3COO)2&amp;middot;nH2O (A, A&amp;rsquo; = Mg, Ca, Sr, Ba, Mn)&lt;/strong&gt;</text>
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                <text>Owing to their potential as single-source precursors for compositionally complex materials, there is growing interest in the rational design of multimetallic compounds containing fluorinated ligands. In this work, we show that chemical and structural principles for a materials-by-design approach to bimetallic trifluoroacetates can be established through a systematic investigation of the crystal-chemistry of their monometallic counterparts. A(CF3COO)2&amp;middot;nH2O (A = Mg, Ca, Sr, Ba, Mn) monometallic trifluoroacetates were employed to demonstrate the feasibility of this approach. The crystal-chemistry of monometallic trifluoroacetates was mapped using variable-temperature single-crystal X-ray diffraction, powder X-ray diffraction, and thermal analysis. The evolution with temperature of the previously unknown crystal structure of Mg(CF3COO)2&amp;middot;4H2O was found to be identical to that of Mn(CF3COO)2&amp;middot;4H2O. More important, the flexibility of Mnx(CF3COO)2x&amp;middot;4H2O (x = 1, 3) to adopt two structures, one isostructural to Mg(CF3COO)2&amp;middot;4H2O, the other isostructural to Ca3(CF3COO)6&amp;middot;4H2O, enabled the synthesis of Mg-Mn and Ca-Mn bimetallic trifluoroacetates. Mg0.45Mn0.55(CF3COO)2&amp;middot;4H2O was found to be isostructural to Mg(CF3COO)2&amp;middot;4H2O and exhibited isolated metal-oxygen octahedra with Mg(2+) and Mn(2+) nearly equally distributed over the metal sites (Mg/Mn: 45/55). Ca1.72Mn1.28(CF3COO)6&amp;middot;4H2O was isostructural to Ca3(CF3COO)6&amp;middot;4H2O and displayed trimers of metal-oxygen corner-sharing octahedra; Ca(2+) and Mn(2+) were unequally distributed over the central (Ca/Mn: 96/4) and terminal (Ca/Mn: 38/62) octahedral sites.</text>
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                <text>Dalton Transactions b. 46, 2017. -- p. 1420-1430</text>
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                <text>The results from the synthesis of peptides by Fmoc/SPPS on a 2-CTC resin and then lactamization in solution or solid phase for the preparation of cyclopeptides are presented. Both procedures allow the synthesis of the desired compounds in good to very good yield and with high cyclization efficiency for on-resin macrocyclization. In addition, the activities of the corresponding cyclopeptides against the chloroquine-resistant K1 strain of Plasmodium falciparum were evaluated. Cyclo-Cys(Trt)-Gly-Thr(tBu)-Gly-Cys(Trt)-Gly showed potent in vitro and selective activity against this parasite, EC50 = 28 nM.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>The results from the synthesis of peptides by Fmoc/SPPS on a 2-CTC resin and then lactamization in solution or solid phase for the preparation of cyclopeptides are presented. Both procedures allow the synthesis of the desired compounds in good to very good yield and with high cyclization efficiency for on-resin macrocyclization. In addition, the activities of the corresponding cyclopeptides against the chloroquine-resistant K1 strain of Plasmodium falciparum were evaluated. Cyclo-Cys(Trt)-Gly-Thr( tBu)-Gly-Cys(Trt)-Gly showed potent in vitro and selective activity against this parasite, EC50 = 28 nM.</text>
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                <text>ACS Combinatorial Science v. 20, no. 4, 2018. -- p. 212-219</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Novel a,a-disubstituted epoxy esters were prepared in enantiopure form by hydrolytic kinetic resolution (HKR) of the corresponding racemic mixtures using chiral salenCo(III) as catalyst. The methodology provides a convenient route to enantioenriched b,c-epoxy esters 2a, 2c and 2d.</text>
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                <text>Monodisperse latex particles with surface amino groups were prepared by a two-step emulsion polymerization. In the first step, the seeds were synthesized by batch emulsion polymerization of styrene; and in the second step, two different aminofunctionalized monomers [aminoethylmethacrylate hydrochloride (AEMH) and vinylbenzylamine hydrochloride (VBAH)], two different initiator systems (K2S2O8 and K2S2O8/Na2S2O5) and mixtures of emulsifiers sodium dodecylsulfate (SDS) and Tween 21 were used to synthesize the final latexes. To characterize the final latexes, conversions were obtained gravimetrically and particle size distributions and average particle diameters were determined by transmission electron microscopy (TEM) and photon correlation spectroscopy (PCS). The amount of amino groups was determined by the SPDP (N-succinimidyl 3-(2-pyridyldithio)propionate) method. The influence of the different conditions used to synthesize the latexes on the colloidal stability of the particles was evaluated by measuring the diameters of the final latexes dispersed in solutions at different pHs and ionic strengths. The most stable latexes were obtained using the smallest seed, VBAH monomer, and the K2S2O8/Na2S2O5 initiator system.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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&lt;p dir="ltr"&gt;&lt;span&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/span&gt;&lt;/p&gt;&#13;
&lt;p dir="ltr"&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derechode autor&lt;/strong&gt;&lt;span&gt;&amp;nbsp;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/span&gt;&lt;/p&gt;&#13;
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                <text>&lt;strong&gt;Synthesis of novel indenoquinolines and indenopyridazines via photoisomerization of benzotropolone derivatives&lt;/strong&gt;</text>
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                <text>We describe the photoisomerization of hetero Diels&amp;ndash;Alder adducts of tetramethylpurpurogallin bearing b,c-unsaturated ketone chromophores and endocyclic &amp;ndash;N&amp;ndash;O&amp;ndash; or &amp;ndash;N&amp;ndash;N&amp;ndash; groups. Based on spectroscopic and crystallographic data, our results indicate that the outcome of the reaction for the two types of substrates can be correlated with the difference in the stabilities of the radical intermediates generated in each case. For oxazines, the photoisomerization involves both the b,c-unsaturated ketone and &amp;ndash;N&amp;ndash;O&amp;ndash; moieties, and proceeds through the formation of allyl, benzoyl, phenyl, and a-carbonyl radical intermediates. While the same allylic and benzoyl radicals are formed in adducts with an &amp;ndash;N&amp;ndash;N&amp;ndash; group, the hydrazine does not participate in the reaction and the product is a simple rearrangement of the initial intermediate.</text>
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                <text>&lt;strong&gt;Tabarez, Carlos&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Waterman, C.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Rapp, A. L.&lt;/strong&gt;</text>
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                <text>&lt;a title="Curr&amp;iacute;culum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=1424ef7476f5da983ef6cd034fcf13fe" target="_blank"&gt;&lt;strong&gt;Moyna, Patrick&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;a title="Curr&amp;iacute;culum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=0933731a43508cea8800ee7ee13daf0a" target="_blank"&gt;&lt;strong&gt;Moyna, Guillermo&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Tetrahedron Letters v. 50, no. 51, 2009. -- p.7128-7131</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI:10.1016/j.tetlet.2009.09.176</text>
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                  <text>Bibliografía Nacional Química</text>
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              <name>Description</name>
              <description>An account of the resource</description>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;Synthesis of Oligosaccharides Derived from Lactulose (OsLu) Using Soluble and Immobilized Aspergillus oryzae &amp;beta;-Galactosidase&lt;/strong&gt;</text>
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                <text>OLIGOSACARIDOS</text>
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                <text>INMOVILIZACION DE ENZIMAS</text>
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                <text>ASPERGILLUS ORYZAE</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>&amp;beta;-Galactosidase from Aspergillus oryzae offers a high yield for the synthesis of oligosaccharides&lt;br /&gt;derived from lactulose (OsLu) by transgalactosylation. Oligosaccharides with&lt;br /&gt;degree of polymerization (DP) &amp;ge; 3 have shown to possess higher in vitro bifidogenic effect&lt;br /&gt;than di- and tetrasaccharides. Thus, in this work, an optimization of reaction conditions&lt;br /&gt;affecting the specific selectivity of A. oryzae &amp;beta;-galactosidase for synthesis of OsLu has&lt;br /&gt;been carried out to enhance OsLu with DP &amp;ge; 3 production. Assays with &amp;beta;-galactosidase&lt;br /&gt;immobilized onto a glutaraldehyde&amp;ndash;agarose support were also carried out with the aim&lt;br /&gt;of making the process cost-effective and industrially viable. Optimal conditions with both&lt;br /&gt;soluble and immobilized enzyme for the synthesis of OsLu with DP &amp;ge; 3 were 50 &amp;deg;C, pH&lt;br /&gt;6.5, 450 g/L of lactulose, and 8 U/mL of enzyme, reaching yields of ca. 50% (w/v) of total&lt;br /&gt;OsLu and ca. 20% (w/v) of OsLu with DP 3, being 6&amp;prime;-galactosyl-lactulose the major one,&lt;br /&gt;after a short reaction time. Selective formation of disaccharides, however, was favored&lt;br /&gt;at 60 &amp;deg;C, pH 4.5, 450 g/L of lactulose and 8 U/mL of enzyme. Immobilization increased&lt;br /&gt;the enzymatic stability to temperature changes and allowed to reuse the enzyme. We&lt;br /&gt;can conclude that the use, under determined optimal conditions, of the A. oryzae &amp;beta;-galactosidase&lt;br /&gt;immobilized on a support of glutaraldehyde&amp;ndash;agarose constitutes an efficient&lt;br /&gt;and cost-effective alternative to the use of soluble &amp;beta;-galactosidases for the synthesis of&lt;br /&gt;prebiotic OsLu mixtures.</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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                <text>&lt;strong&gt;Cardelle-Cobas, Alejandra&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Olano, Agust&amp;iacute;n&lt;/strong&gt;</text>
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                <text>&lt;a title="Curr&amp;iacute;culum vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=da4f071f890fec490234707830d5f695" target="_blank"&gt;&lt;strong&gt;Irazoqui, Gabriela&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;a title="Curr&amp;iacute;culum vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=3c8a423235a59fcbc901eec52b2b7794" target="_blank"&gt;&lt;strong&gt;Giacomini, Cecilia&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;a title="Curr&amp;iacute;culum vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=8dfa5283acaafc5c73dab5b61b04f9a0" target="_blank"&gt;&lt;strong&gt;Batista-Viera, Francisco&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Corzo, Nieves&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Corzo Mart&amp;iacute;nez, Marta&lt;/strong&gt;</text>
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                <text>Frontiers in Bioengineering and Biotechnology v. 4, 2016. -- 10p.- e21</text>
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                <text>Elsevier</text>
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            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="356332">
                <text>&lt;p align="LEFT"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p style="margin-bottom: 0cm;"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>http://dx.doi.org/10.1016/j.apradiso.2015.12.051</text>
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        <name>Inmovilización de enzimas</name>
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        <name>Oligosacaridos</name>
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