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"One-pot" synthesis of carbamates via curtius rearrangement

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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


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