OME REACTIONS 0F NN - DISUBSTITUTED THIOAMIDES

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dc.contributor.authorOKECHA, STEPHEN AGWO
dc.date.accessioned2017-02-07T07:51:53Z
dc.date.available2017-02-07T07:51:53Z
dc.date.issued1973-01
dc.descriptionA THESIS PRESENTED TO THE AHMADU BELLO UNIVERSITY FOR THE DEGREE OF MASTER OF SCIENCE DEPARTMENT OF CHEMISTRY, AHMADU BELLO UNIVERSITY, ZARIA.en_US
dc.description.abstractIn the present work some of the synthetic applications of S-alkyl quaternary salts of NK-disub¬stituted thioamides were investigated, NN-Disubstituted tliioamides which were prepared by the Willgerodt Klndler procedure, 1-8 or from the amides with phosphorus pentasulphide9 were reacted With simple alkyl halides to give S-alkyl quaternary salts in good yields. The reaction of the quaternary salts With hydroxy 1amine hydrochloride produced NN-disubstituted amidoximes, while treatment of the quaternary salts with potassium cyanide gave novel S-alkyl quaternary cyanides some of which hydrolysed to cyanoamides under surprisingly mild conditionsen_US
dc.identifier.urihttp://hdl.handle.net/123456789/8659
dc.language.isoenen_US
dc.subjectREACTIONS,en_US
dc.subjectNN - DISUBSTITUTED THIOAMIDES,en_US
dc.titleOME REACTIONS 0F NN - DISUBSTITUTED THIOAMIDESen_US
dc.typeThesisen_US
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