<?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>S1870-249X2010000300006</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Synthesis of Peptides Histamine H2 Receptors in Solid-Phase Assisted by Microwave]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Reynoso-Soto]]></surname>
<given-names><![CDATA[Edgar A.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rivero]]></surname>
<given-names><![CDATA[Ignacio A.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Investigación del Instituto Tecnológico de Tijuana  ]]></institution>
<addr-line><![CDATA[Tijuana B.C]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Instituto Nacional de Investigaciones Nucleares Departamento de Química ]]></institution>
<addr-line><![CDATA[México D.F]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2010</year>
</pub-date>
<volume>54</volume>
<numero>3</numero>
<fpage>160</fpage>
<lpage>163</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2010000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2010000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2010000300006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[The synthesis of histamine H2 receptors peptides was conducted using the methodology of solid phase assisted by microwaves. Microwaves can reduce the reaction times during the coupling and deprotection steps to obtain the desired peptide sequence. The coupling reaction was carried out with a mixture of N, N'-diisopropyl-carbodiimide (DIC) and N,N,N'N'-tetramethyl-O-(1H-benzotriazol-1-yl)uronium hexafluorophosphate (HBTU). The purity and yield are improved in peptide synthesis assisted by microwaves. Coupling reactions and deprotection on Rink resin were carried out in 5 min depending on amino acid and the length of the peptide chain.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[La síntesis de péptidos receptores de histamina H2 fue realizada empleando la metodología de síntesis en fase sólida asistida por microondas. Las microondas permitieron disminuir los tiempos de reacción durante las etapas acoplamiento y desprotección para obtener la secuencia deseada de péptido. La reacción de acoplamiento se llevó a cabo con una mezcla de N, N'-diisopripilcarbodimida y N,N,N',N'-tetrarnetil-O-(1H-benzotriazol-1-il)uronio hexafluorofosfato. La pureza y el rendimiento son mejorados en la síntesis de péptidos asistida por microondas. Las reacciones de acoplamiento y desprotección sobre la resina de Rink se llevaron a cabo en 5 min por protocolo y dependiendo del aminoácido son el número de protocolos empleados.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Solid Phase]]></kwd>
<kwd lng="en"><![CDATA[Peptide]]></kwd>
<kwd lng="en"><![CDATA[Microwave]]></kwd>
<kwd lng="es"><![CDATA[Fase sólida]]></kwd>
<kwd lng="es"><![CDATA[péptidos]]></kwd>
<kwd lng="es"><![CDATA[microondas]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Synthesis of Peptides Histamine H2 Receptors in Solid&#150;Phase Assisted by Microwave</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Edgar A. Reynoso&#150;Soto<sup>1</sup> and Ignacio A. Rivero<sup>1,2 *</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>1</sup> Centro de Graduados e Investigaci&oacute;n del Instituto Tecnol&oacute;gico de Tijuana. Apartado Postal 1166, Tijuana, B.C. 22000 M&eacute;xico. <sup>*</sup>Responsible author:</i> <a href="mailto:irivero@tectijuana.mx">irivero@tectijuana.mx</a>.</font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>2</sup> Instituto Nacional de Investigaciones Nucleares, Departamento de Qu&iacute;mica. Carretera M&eacute;xico Toluca S/N, La Marquesa, Ocoyoacac 52750, M&eacute;xico, D.F.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Received January 6, 2009    ]]></body>
<body><![CDATA[<br>   Accepted May 29, 2010</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">The synthesis of histamine H2 receptors peptides was conducted using the methodology of solid phase assisted by microwaves. Microwaves can reduce the reaction times during the coupling and deprotection steps to obtain the desired peptide sequence. The coupling reaction was carried out with a mixture of <i>N, N'</i>&#150;diisopropyl&#150;carbodiimide (DIC) and <i>N,N,N'N'</i>&#150;tetramethyl&#150;O&#150;(1<i>H</i>&#150;benzotriazol&#150;1&#150;yl)uronium hexafluorophosphate (HBTU). The purity and yield are improved in peptide synthesis assisted by microwaves. Coupling reactions and deprotection on Rink resin were carried out in 5 min depending on amino acid and the length of the peptide chain.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Solid Phase, Peptide, Microwave.</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">La s&iacute;ntesis de p&eacute;ptidos receptores de histamina H2 fue realizada empleando la metodolog&iacute;a de s&iacute;ntesis en fase s&oacute;lida asistida por microondas. Las microondas permitieron disminuir los tiempos de reacci&oacute;n durante las etapas acoplamiento y desprotecci&oacute;n para obtener la secuencia deseada de p&eacute;ptido. La reacci&oacute;n de acoplamiento se llev&oacute; a cabo con una mezcla de <i>N, N'</i>&#150;diisopripilcarbodimida y <i>N,N,N',</i>N'&#150;tetrarnetil&#150;O&#150;(1<i>H</i>&#150;benzotriazol&#150;1&#150;il)uronio hexafluorofosfato. La pureza y el rendimiento son mejorados en la s&iacute;ntesis de p&eacute;ptidos asistida por microondas. Las reacciones de acoplamiento y desprotecci&oacute;n sobre la resina de Rink se llevaron a cabo en 5 min por protocolo y dependiendo del amino&aacute;cido son el n&uacute;mero de protocolos empleados.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Fase s&oacute;lida, p&eacute;ptidos, microondas.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><a href="/pdf/jmcs/v54n3/v54n3a6.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgements</b></font></p>     <p align="justify"><font face="verdana" size="2">We are grateful to Consejo Nacional de Ciencia y Tecnolog&iacute;a, M&eacute;xico (CONACyT, grant No. SEP&#150;2004&#150;CO1&#150;47895) and Direcci&oacute;n General de Educaci&oacute;n Superior Tecnol&oacute;gica (DGEST) for support this project. Edgar A. Reynoso thanks CONACYT for a graduate scholarship.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>References</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. (a) Barker, R. <i>Organic Chemistry of Biological Compounds, </i>Prentice&#150;Hall, Englewood Cliffs, 1971.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942799&pid=S1870-249X201000030000600001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> (b) Bladon, C. <i>The Chemistry of Natural Products, </i>Thomsom R. H. Ed, Blackie Academic and Professional (Chapman&#150;Hall), Glasgow, 1993.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942800&pid=S1870-249X201000030000600002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">2. Rivero, I. A.; Gonz&aacute;lez, T.; Basterrechea, M. <i>Rev. Soc. Qu&iacute;m. M&eacute;x. </i><b>2004, </b><i>48, </i>310&#150;314.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942802&pid=S1870-249X201000030000600003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">3. (a) Merrifield, R. B.; Mitchell, A. R.; Clarke, J. E. <i>J. Org. Chem. </i><b>1974, </b><i>39, </i>660&#150;668.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942804&pid=S1870-249X201000030000600004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> (b) Yu, H. M.; Chen, S. T.; Wang, K. <i>J. Org. Chem. </i><b>1992, </b><i>57, </i>4781&#150;4784.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942805&pid=S1870-249X201000030000600005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">4. (a) Stadler, A.; Kappe, C. O. <i>Eur. J. Org. Chem. </i><b>2001, </b>919&#150;925.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942807&pid=S1870-249X201000030000600006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> (b) Stadler, A.; Kappe, C. O. <i>Tetrahedron </i><b>2001, </b><i>57, </i>3915&#150;3920.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942808&pid=S1870-249X201000030000600007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --> (c) Leadbeater, N. E.; Torenius, H. M. <i>J. Org. Chem. </i><b>2002, </b><i>67, </i>3145&#150;3148.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942809&pid=S1870-249X201000030000600008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">5. Soriano&#150;Mora, J. M. Nuevos reactivos polim&eacute;ricos para el acoplamiento y protecci&oacute;n de amino&aacute;cidos, Tesis doctoral, Facultad de Ciencias, Universidad de Alicante, 2002, p19.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942811&pid=S1870-249X201000030000600009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     ]]></body>
<body><![CDATA[<!-- ref --><p align="justify"><font face="verdana" size="2">6. DeTar, D. F.; Silverstein, R. <i>J. Am. Chem. Soc. </i><b>1966, </b>88, 1020&#150;1023.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942813&pid=S1870-249X201000030000600010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">7. Arendt, A.; Kolodziejczyk, A. M. <i>Tetrahedron Lett. </i><b>1978, </b><i>19, </i>3867&#150;3868.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942815&pid=S1870-249X201000030000600011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">8. Scott, F. L.; Glick, R. E.; Winstein, S. <i>Experientia </i><b>1957, </b>13, 183&#150;185.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942817&pid=S1870-249X201000030000600012&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">9. Albericio, F.; Chinchilla, R.; Dodsworth, D. J.; N&aacute;jera, C. <i>Org. Prep. Proc. Int. </i><b>2001, </b><i>33, </i>203&#150;304.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942819&pid=S1870-249X201000030000600013&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">10. Bishnu, P. J.; Park, J. P.; Kim, J. M., Lohani, C. R.; Cho, H.; Lee, K. H. <i>Tetrahedron Lett. </i><b>2008, </b>49, 98&#150;101.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942821&pid=S1870-249X201000030000600014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     ]]></body>
<body><![CDATA[<!-- ref --><p align="justify"><font face="verdana" size="2">11. Black, J. W.; Duncan, W. A. M.; Durant, C. J.; Ganellin, C. R.: Parsons, E. M. <i>Nature </i><b>1972, </b><i>236, </i>385&#150;390.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942823&pid=S1870-249X201000030000600015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">12. Durant, G. J.; Ganellin, C. R.; Parson, M. E. <i>J. Med. Chern. </i><b>1975, </b><i>18, </i>905&#150;909</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942825&pid=S1870-249X201000030000600016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">13. Weinstein, H.; Chou, D.; Johnson, C. L.; Kang, S.; Green, J. P. <i>Mol. Pharmacol. </i><b>1976, </b>12, 738&#150;745.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942826&pid=S1870-249X201000030000600017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">14. Gantz, I.; DelValle, J.; Wang, L.&#150;d.; Tashiro, T.; Munzert, G.; Guo, Y.&#150;J. Konda, Y.; Yamada, T. <i>J. Biol. Chem. </i>1992, 267, 20840&#150;20843.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942828&pid=S1870-249X201000030000600018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">15. Rivero, I.A.; Gonz&aacute;lez, T.; Pina&#150;Luis, G.; D&iacute;az&#150;Garcia M. E. <i>J. Comb. Chem. </i><b>2005, </b>7, 46&#150;53.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4942830&pid=S1870-249X201000030000600019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>      ]]></body><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Barker]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<source><![CDATA[Organic Chemistry of Biological Compounds]]></source>
<year>1971</year>
<publisher-loc><![CDATA[Englewood Cliffs ]]></publisher-loc>
<publisher-name><![CDATA[Prentice-Hall]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B2">
<nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bladon]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Thomsom]]></surname>
<given-names><![CDATA[R. H]]></given-names>
</name>
</person-group>
<source><![CDATA[The Chemistry of Natural Products]]></source>
<year>1993</year>
<publisher-loc><![CDATA[Chapman-Hall^eGlasgow Glasgow]]></publisher-loc>
<publisher-name><![CDATA[Blackie Academic and Professional]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B3">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rivero]]></surname>
<given-names><![CDATA[I. A]]></given-names>
</name>
<name>
<surname><![CDATA[González]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Basterrechea]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<source><![CDATA[Rev. Soc. Quím. Méx]]></source>
<year>2004</year>
<volume>48</volume>
<page-range>310-314</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Merrifield]]></surname>
<given-names><![CDATA[R. B]]></given-names>
</name>
<name>
<surname><![CDATA[Mitchell]]></surname>
<given-names><![CDATA[A. R]]></given-names>
</name>
<name>
<surname><![CDATA[Clarke]]></surname>
<given-names><![CDATA[J. E]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Org. Chem]]></source>
<year>1974</year>
<volume>39</volume>
<page-range>660-668</page-range></nlm-citation>
</ref>
<ref id="B5">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Yu]]></surname>
<given-names><![CDATA[H. M]]></given-names>
</name>
<name>
<surname><![CDATA[Chen]]></surname>
<given-names><![CDATA[S. T]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Org. Chem]]></source>
<year>1992</year>
<volume>57</volume>
<page-range>4781-4784</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stadler]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Kappe]]></surname>
<given-names><![CDATA[C. O]]></given-names>
</name>
</person-group>
<source><![CDATA[Eur. J. Org. Chem]]></source>
<year>2001</year>
<page-range>919-925</page-range></nlm-citation>
</ref>
<ref id="B7">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stadler]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Kappe]]></surname>
<given-names><![CDATA[C. O]]></given-names>
</name>
</person-group>
<source><![CDATA[Tetrahedron]]></source>
<year>2001</year>
<volume>57</volume>
<page-range>3915-3920</page-range></nlm-citation>
</ref>
<ref id="B8">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Leadbeater]]></surname>
<given-names><![CDATA[N. E]]></given-names>
</name>
<name>
<surname><![CDATA[Torenius]]></surname>
<given-names><![CDATA[H. M]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Org. Chem]]></source>
<year>2002</year>
<volume>67</volume>
<page-range>3145-3148</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>5</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Soriano-Mora]]></surname>
<given-names><![CDATA[J. M]]></given-names>
</name>
</person-group>
<source><![CDATA[Nuevos reactivos poliméricos para el acoplamiento y protección de aminoácidos]]></source>
<year></year>
<page-range>19</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[DeTar]]></surname>
<given-names><![CDATA[D. F]]></given-names>
</name>
<name>
<surname><![CDATA[Silverstein]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Am. Chem. Soc]]></source>
<year>1966</year>
<volume>88</volume>
<page-range>1020-1023</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Arendt]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Kolodziejczyk]]></surname>
<given-names><![CDATA[A. M]]></given-names>
</name>
</person-group>
<source><![CDATA[Tetrahedron Lett.]]></source>
<year>1978</year>
<volume>19</volume>
<page-range>3867-3868</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Scott]]></surname>
<given-names><![CDATA[F. L]]></given-names>
</name>
<name>
<surname><![CDATA[Glick]]></surname>
<given-names><![CDATA[R. E]]></given-names>
</name>
<name>
<surname><![CDATA[Winstein]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<source><![CDATA[Experientia]]></source>
<year>1957</year>
<volume>13</volume>
<page-range>183-185</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Albericio]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Chinchilla]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Dodsworth]]></surname>
<given-names><![CDATA[D. J]]></given-names>
</name>
<name>
<surname><![CDATA[Nájera]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
</person-group>
<source><![CDATA[Org. Prep. Proc. Int]]></source>
<year>2001</year>
<volume>33</volume>
<page-range>203-304</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bishnu]]></surname>
<given-names><![CDATA[P. J]]></given-names>
</name>
<name>
<surname><![CDATA[Park]]></surname>
<given-names><![CDATA[J. P]]></given-names>
</name>
<name>
<surname><![CDATA[Kim]]></surname>
<given-names><![CDATA[J. M]]></given-names>
</name>
<name>
<surname><![CDATA[Lohani]]></surname>
<given-names><![CDATA[C. R]]></given-names>
</name>
<name>
<surname><![CDATA[Cho]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Lee]]></surname>
<given-names><![CDATA[K. H]]></given-names>
</name>
</person-group>
<source><![CDATA[Tetrahedron Lett]]></source>
<year>2008</year>
<volume>49</volume>
<page-range>98-101</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Black]]></surname>
<given-names><![CDATA[J. W]]></given-names>
</name>
<name>
<surname><![CDATA[Duncan]]></surname>
<given-names><![CDATA[W. A. M]]></given-names>
</name>
<name>
<surname><![CDATA[Durant]]></surname>
<given-names><![CDATA[C. J]]></given-names>
</name>
<name>
<surname><![CDATA[Ganellin]]></surname>
<given-names><![CDATA[C. R]]></given-names>
</name>
<name>
<surname><![CDATA[Parsons]]></surname>
<given-names><![CDATA[E. M]]></given-names>
</name>
</person-group>
<source><![CDATA[Nature]]></source>
<year>1972</year>
<volume>236</volume>
<page-range>385-390</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Durant]]></surname>
<given-names><![CDATA[G. J]]></given-names>
</name>
<name>
<surname><![CDATA[Ganellin]]></surname>
<given-names><![CDATA[C. R]]></given-names>
</name>
<name>
<surname><![CDATA[Parson]]></surname>
<given-names><![CDATA[M. E]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Med. Chern]]></source>
<year>1975</year>
<volume>18</volume>
<page-range>905-909</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Weinstein]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Chou]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Johnson]]></surname>
<given-names><![CDATA[C. L]]></given-names>
</name>
<name>
<surname><![CDATA[Kang]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Green]]></surname>
<given-names><![CDATA[J. P]]></given-names>
</name>
</person-group>
<source><![CDATA[Mol. Pharmacol]]></source>
<year>1976</year>
<volume>12</volume>
<page-range>738-745</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>14</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gantz]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[DelValle]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[L.-d]]></given-names>
</name>
<name>
<surname><![CDATA[Tashiro]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Munzert]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Guo]]></surname>
<given-names><![CDATA[Y.-J]]></given-names>
</name>
<name>
<surname><![CDATA[Konda]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
<name>
<surname><![CDATA[Yamada]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Biol. Chem]]></source>
<year>1992</year>
<volume>267</volume>
<page-range>20840-20843</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rivero]]></surname>
<given-names><![CDATA[I.A]]></given-names>
</name>
<name>
<surname><![CDATA[González]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Pina-Luis]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Díaz-Garcia]]></surname>
<given-names><![CDATA[M. E]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Comb. Chem]]></source>
<year>2005</year>
<volume>7</volume>
<page-range>46-53</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
