dc.contributor.author |
Kyei-Baffour, Kwaku |
en_US |
dc.date.accessioned |
2014-12-05T15:00:21Z |
|
dc.date.accessioned |
2019-09-08T02:52:40Z |
|
dc.date.available |
2014-12-05T15:00:21Z |
|
dc.date.available |
2019-09-08T02:52:40Z |
|
dc.date.issued |
2014 |
|
dc.identifier |
896823160 |
en_US |
dc.identifier.other |
b21497072 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/1989/11404 |
|
dc.description |
ix, 93 leaves : illustrations ; 29 cm. |
en_US |
dc.description.abstract |
In this thesis, acyl chlorides were successfully converted to their corresponding carbamates via Curtius rearrangement in a novel one-pot synthesis procedure that uses p-nitrobenzenesulfonylazide as the azide nucleophile source. In the process alkyl esters were also synthesized as the associated by-product. The thesis also deals with the one-pot synthesis of acyl azides from acyl chlorides. |
en_US |
dc.description.statementofresponsibility |
by Kwaku Kyei-Baffour. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.relation.ispartofseries |
Master's Theses no. 1467 |
en_US |
dc.subject.lcsh |
Organic compounds--Synthesis. |
en_US |
dc.subject.lcsh |
Azides. |
en_US |
dc.subject.lcsh |
Carbamates. |
en_US |
dc.subject.lcsh |
Rearrangements (Chemistry)--Chemistry, Organic. |
en_US |
dc.title |
"One-pot" synthesis of carbamates via curtius rearrangement |
en_US |
dc.type |
Thesis |
en_US |