Reactions of Lead Tetraacetate. II. Formation of Carbamic Acid Esters from Primary Carboxamides

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dc.contributor.authorHassanali, Ahmed
dc.contributor.authorAcott, B.
dc.contributor.authorBeckwith, A. L. J.
dc.date.accessioned2014-03-04T08:22:26Z
dc.date.available2014-03-04T08:22:26Z
dc.date.issued1968
dc.descriptiondoi:10.1071/CH9680197en_US
dc.description.abstractTreatment of primary carboxamides with lead tetraacetate in benzene-alcohol mixtures or neat alcohol affords a convenient, flexible, and efficient method for the preparation of N-substituted carbamic acid esters. The reaction is applicable to amides and alcohols of a wide range of structural types including compounds containing oleflnic, ester, aromatic, and other reactive functions. The reaction mechanism appears to involve intermediate formation of isocyanates.en_US
dc.identifier.citationAustralian Journal of Chemistry 21(1) 197 - 205en_US
dc.identifier.urihttp://ir-library.ku.ac.ke/handle/123456789/9180
dc.language.isoenen_US
dc.publisherCSIRO Publishingen_US
dc.titleReactions of Lead Tetraacetate. II. Formation of Carbamic Acid Esters from Primary Carboxamidesen_US
dc.typeArticleen_US
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