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 |