{"id":{"repo_id":"kennesaw","oai_identifier":"oai:digitalcommons.kennesaw.edu:mscs_etd-1010"},"canonical_url":"https://search.dev.ndltd.org/etd/kennesaw/oai:digitalcommons.kennesaw.edu:mscs_etd-1010","repository":{"repo_id":"kennesaw","name":"Kennesaw State University","base_url":"https://digitalcommons.kennesaw.edu/do/oai/"},"display":{"title":"Synthetic Methods for the Preparation of 1,3-S,O-Esters, α-Phosphonovinyl Triflates, and α-Alkynylphosphonates","abstract":"<p>A broad and systematic study was conducted on synthetic methods to efficiently synthesize 1,3-<em>S</em>,<em>O</em>-esters, α-phosphonovinyl triflates, and α-alkynylphosphonates under mild reaction conditions. The master’s thesis is composed of two projects; the first project is titled “Synthesis of 1,3-<em>S</em>,<em>O</em>-Esters” and the second project is titled “Synthesis of α-Phosphonovinyl Triflates and α-Alkynylphosphonates.” The first project outlines a synthetic route to conveniently prepare novel α-functionalized 1,3-<em>S</em>,<em>O</em>-esters via an acid-promoted hydrolysis of α-functionalized α-oxoketene dimethylthioacetals. The second project, unrelated to the first project, primarily focuses on extensive synthetic methodology developed to prepare novel β-functionalized α-phosphonovinyl triflates and display their synthetic application by performing a base-promoted β-elimination to produce β-functionalized α-alkynylphosphonates.</p>","abstract_html":"&lt;p&gt;A broad and systematic study was conducted on synthetic methods to efficiently synthesize 1,3-&lt;em&gt;S&lt;/em&gt;,&lt;em&gt;O&lt;/em&gt;-esters, α-phosphonovinyl triflates, and α-alkynylphosphonates under mild reaction conditions. The master’s thesis is composed of two projects; the first project is titled “Synthesis of 1,3-&lt;em&gt;S&lt;/em&gt;,&lt;em&gt;O&lt;/em&gt;-Esters” and the second project is titled “Synthesis of α-Phosphonovinyl Triflates and α-Alkynylphosphonates.” The first project outlines a synthetic route to conveniently prepare novel α-functionalized 1,3-&lt;em&gt;S&lt;/em&gt;,&lt;em&gt;O&lt;/em&gt;-esters via an acid-promoted hydrolysis of α-functionalized α-oxoketene dimethylthioacetals. The second project, unrelated to the first project, primarily focuses on extensive synthetic methodology developed to prepare novel β-functionalized α-phosphonovinyl triflates and display their synthetic application by performing a base-promoted β-elimination to produce β-functionalized α-alkynylphosphonates.&lt;/p&gt;","abstract_has_math":false,"creators":["Kercher, David P"],"institution":null,"degree_name":"Master of Science in Chemical Sciences (MSCB)","degree_level":"Thesis","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Dr. Christopher W. Alexander","Dr. John Haseltine","Dr. Ellen Moomaw"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2016,"date_issued":"2016-04-29T07:00:00Z","date_published":"2016-04-29T07:00:00Z","updated_at":"2026-07-24T02:43:09Z","subjects":["1","3-S","O-esters","α-oxoketene dimethylthioacetal","Amberlyst-15","α-ketophosphonate","α-alkynylphosphonate","α-phosphonovinyl triflates","Chemistry","Organic Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.kennesaw.edu/mscs_etd/11","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Dr. Christopher W. 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The master’s thesis is composed of two projects; the first project is titled “Synthesis of 1,3-<em>S</em>,<em>O</em>-Esters” and the second project is titled “Synthesis of α-Phosphonovinyl Triflates and α-Alkynylphosphonates.” The first project outlines a synthetic route to conveniently prepare novel α-functionalized 1,3-<em>S</em>,<em>O</em>-esters via an acid-promoted hydrolysis of α-functionalized α-oxoketene dimethylthioacetals. The second project, unrelated to the first project, primarily focuses on extensive synthetic methodology developed to prepare novel β-functionalized α-phosphonovinyl triflates and display their synthetic application by performing a base-promoted β-elimination to produce β-functionalized α-alkynylphosphonates.</p>"]},{"key":"dc:title","label":"Title","values":["Synthetic Methods for the Preparation of 1,3-S,O-Esters, α-Phosphonovinyl Triflates, and α-Alkynylphosphonates"]}]}],"canonical_facts":{"dc:contributor":["Dr. Christopher W. Alexander","Dr. John Haseltine","Dr. Ellen Moomaw"],"dc:creator":["Kercher, David P"],"dc:date.available":["2021-06-09T07:00:00Z"],"dc:description.abstract":["<p>A broad and systematic study was conducted on synthetic methods to efficiently synthesize 1,3-<em>S</em>,<em>O</em>-esters, α-phosphonovinyl triflates, and α-alkynylphosphonates under mild reaction conditions. The master’s thesis is composed of two projects; the first project is titled “Synthesis of 1,3-<em>S</em>,<em>O</em>-Esters” and the second project is titled “Synthesis of α-Phosphonovinyl Triflates and α-Alkynylphosphonates.” The first project outlines a synthetic route to conveniently prepare novel α-functionalized 1,3-<em>S</em>,<em>O</em>-esters via an acid-promoted hydrolysis of α-functionalized α-oxoketene dimethylthioacetals. The second project, unrelated to the first project, primarily focuses on extensive synthetic methodology developed to prepare novel β-functionalized α-phosphonovinyl triflates and display their synthetic application by performing a base-promoted β-elimination to produce β-functionalized α-alkynylphosphonates.</p>"],"dc:identifier":["https://digitalcommons.kennesaw.edu/mscs_etd/11"],"dc:subject":["1","3-S","O-esters","α-oxoketene dimethylthioacetal","Amberlyst-15","α-ketophosphonate","α-alkynylphosphonate","α-phosphonovinyl triflates","Chemistry","Organic Chemistry"],"dc:title":["Synthetic Methods for the Preparation of 1,3-S,O-Esters, α-Phosphonovinyl Triflates, and α-Alkynylphosphonates"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science in Chemical Sciences (MSCB)"]},"updated_at":"2026-07-24T02:43:09Z"}