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Synthesis and use of dienyl phosphates in the Suzuki coupling /

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dc.contributor.author Grote, Matthew P. en_US
dc.contributor.author Youngstown State University. Dept. of Chemistry. en_US
dc.date.accessioned 2011-01-31T14:16:54Z
dc.date.accessioned 2019-09-08T02:30:06Z
dc.date.available 2011-01-31T14:16:54Z
dc.date.available 2019-09-08T02:30:06Z
dc.date.created 2002 en_US
dc.date.issued 2002 en_US
dc.identifier 51027999 en_US
dc.identifier.other b19007620 en_US
dc.identifier.uri http://jupiter.ysu.edu/record=b1900762 en_US
dc.identifier.uri http://hdl.handle.net/1989/6120
dc.description xii, 96 leaves : ill. ; 29 cm. en_US
dc.description Thesis (M.S.)--Youngstown State University, 2002. en_US
dc.description Includes bibliographical references (leaves 66-68). en_US
dc.description.abstract The research presented here is a study of the synthesis of bis(2,2,2-trifluoroethyl) vinyl and dienyl phosphates, and their respective reactivities in two well-known coupling reactions. The required vinyl phosphates can be synthesized by known methods, and this methodology can be extended to dienyl phosphates with only a few slight modifications. Bis(2,2,2-trifluoroethyl) vinyl phosphates are shown to be inadequate starting materials for cross coupling reactions when palladium catalysis is used. Nickel catalysis is shown to be moderately effective as a cross coupling catalyst, providing a methodological basis for the synthesis of new aryl substituted diene systems. en_US
dc.description.statementofresponsibility by Matthew P. Grote. en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses no. 0752 en_US
dc.subject.classification Master's Theses no. 0752 en_US
dc.subject.lcsh Polyphosphates--Synthesis. en_US
dc.title Synthesis and use of dienyl phosphates in the Suzuki coupling / en_US
dc.type Thesis en_US


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