<?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>2026-09-22T08:08:19Z</responseDate><request verb="GetRecord" identifier="oai:ruor.uottawa.ca:10393/28552" metadataPrefix="oai_dc">https://ruor.uottawa.ca/server/oai/request</request><GetRecord><record><header><identifier>oai:ruor.uottawa.ca:10393/28552</identifier><datestamp>2024-02-23T09:00:42Z</datestamp><setSpec>com_10393_242</setSpec><setSpec>col_10393_244</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Synthesis of Single Isomer Trisubstituted Olefins from beta-chloro-alpha-iodo-alpha, beta-Unsaturated Esters and Alkynyl Esters</dc:title>
   <dc:creator>Rajagopal, Thivisa</dc:creator>
   <dc:subject>Chemistry, Organic.</dc:subject>
   <dc:description>A convenient method to synthesize regiospecific and stereoselective trisubstituted olefins bearing three substitutents with various functionalities is disclosed. A unique olefin template such as (E)-beta-chloro-alpha-iodo-alpha,beta-unsaturated esters cross-couple with 9-alkyl-9-BBN to produce single isomer trisubstituted olefins using palladium-catalyzed Suzuki-Miyaura cross-coupling reaction. This methodology can be further expanded to introduce various alkyl groups at the beta-position. The mechanism is somewhat unusual as it involves two catalytic cycles with an allenoate intermediate to explain the observed stereochemistry and protonolysis of that intermediate produces the key product, (E)-beta-chloro-alpha,beta-unsaturated ester. The protonolysis is mediated by the presence of H2O in the inorganic base, K3PO4&amp;amp;middot;H2O.*
Similarly, another method has been developed to synthesize trisubstituted olefins using the alkynyl ester and 9-alkyl-9-BBN. This process also has a broad scope to introduce various alkyl groups at the beta-position. The mechanism currently proposed involves an oxidation of palladium to form H-[Pd]-OH species. This was confirmed based on the importance of water in the catalytic system and the isotopic experiments also confirmed the olefinic hydrogen at the alpha-position arises from the water itself. Following the formation of H-[Pd]-OH, syn carbopalladation to the alkynyl ester creates the hydroxyl palladium vinyl intermediate. However, this mechanism does not explain the observed stereochemistry. A more detailed study is required regarding this mechanism.*
*Please refer to dissertation for diagrams.</dc:description>
   <dc:date>2013-11-07T19:30:21Z</dc:date>
   <dc:date>2013-11-07T19:30:21Z</dc:date>
   <dc:date>2010</dc:date>
   <dc:date>2010</dc:date>
   <dc:type>Thesis</dc:type>
   <dc:identifier>Source: Masters Abstracts International, Volume: 49-02, page: 1188.</dc:identifier>
   <dc:identifier>http://hdl.handle.net/10393/28552</dc:identifier>
   <dc:identifier>http://dx.doi.org/10.20381/ruor-19328</dc:identifier>
   <dc:language>en</dc:language>
   <dc:format>209 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>University of Ottawa (Canada)</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>