<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-21T10:10:39Z</responseDate><request verb="GetRecord" identifier="oai:wakespace.lib.wfu.edu:10339/36145" metadataPrefix="dim">https://wakespace.lib.wfu.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:null:10339/36145</identifier><datestamp>2026-09-18T14:13:13Z</datestamp><setSpec>com_10339_14934</setSpec><setSpec>col_10339_38132</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Junker, Christopher Sean</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2011-09-08T08:35:48Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2013-09-08T08:30:07Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://wakespace.lib.wfu.edu/handle/10339/36145</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Two of the major focuses in current synthetic organic chemistry are asymmetric carbon-carbon bond forming processes and catalytic one-pot reactions.  Two processes that are of interest to our research are the Diels-Alder reaction and transition-metal-catalyzed cross-coupling reactions.  Issues that arise in these processes include poor efficiency and poor stereoselectivity.  My dissertation research has centered around the synthesis and use of 2-silicon-substituted 1,3-dienes to alleviate these problems.  These dienes, whether utilized as reagents or intermediates, serve as synthons for less reactive/selective 2-aryl 1,3-dienes.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Wake Forest University</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Cross-Coupling</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Cycloaddition</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Metathesis</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Multicomponent</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Silane</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Stereoselective</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Dissertation</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeChair" lang="en_US">Welker, Mark E</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Jones, Bradley T</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Jones, Paul B</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">King, Stephen B</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Miller, Craig H</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="discipline" lang="en_US">Chemistry</dim:field>
   <dim:field mdschema="thesis" element="embargo" qualifier="terms" lang="en_US">2013-09-08</dim:field>
   <dim:field mdschema="others" element="access-status">restricted</dim:field>
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