dc.contributor.author |
Carlisle, Lemuel R., II. |
en_US |
dc.contributor.author |
Youngstown State University. Dept. of Chemistry. |
en_US |
dc.date.accessioned |
2011-01-31T14:16:32Z |
|
dc.date.accessioned |
2019-09-08T02:35:53Z |
|
dc.date.available |
2011-01-31T14:16:32Z |
|
dc.date.available |
2019-09-08T02:35:53Z |
|
dc.date.created |
2007 |
en_US |
dc.date.issued |
2007 |
en_US |
dc.identifier.other |
b20242153 |
en_US |
dc.identifier.uri |
http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198202999 |
en_US |
dc.identifier.uri |
http://jupiter.ysu.edu/record=b2024215 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/1989/6086 |
|
dc.description |
viii, 76 p. : ill. ; 29 cm. |
en_US |
dc.description |
Thesis (M.S.)--Youngstown State University, 2007. |
en_US |
dc.description |
Thesis (M.S.)--Youngstown State University, 2008. |
en_US |
dc.description |
Includes bibliographical references (leaves ). |
en_US |
dc.description.abstract |
The synthesis of several phosphonate esters via reaction of the salt of bis(2,2,2-trifluroethyl) phosphite and a given alpha halo carbonyl compound in a Michaelis-Becker reaction scheme. As an alternative to the use of strong base, we employed cesium carbonate as a mild reagent in hopes of successfully synthesizing our target compounds in high yields. |
en_US |
dc.description.statementofresponsibility |
by Lemuel R. Carlisle II. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.relation.ispartofseries |
Master's Theses no. 0970 |
en_US |
dc.subject.classification |
Master's Theses no. 0970 |
en_US |
dc.subject.lcsh |
Phosphonates. |
en_US |
dc.subject.lcsh |
Esters. |
en_US |
dc.subject.lcsh |
Chemistry, Organic. |
en_US |
dc.title |
Novel approaches toward the synthesis of bis(2,2,2-trifluroethoxy) phosphono esters / |
en_US |
dc.type |
Thesis |
en_US |