Please use this identifier to cite or link to this item: http://localhost:8081/jspui/handle/123456789/21456
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPundir, Manish-
dc.date.accessioned2026-09-17T10:52:46Z-
dc.date.available2026-09-17T10:52:46Z-
dc.date.issued2022-04-
dc.identifier.urihttp://localhost:8081/jspui/handle/123456789/21456-
dc.guideSharma, Anujen_US
dc.description.abstractThis dissertation describes the method of preparation of α-aryl keto acids which are used as acylating reagents in organic synthesis. The aryl α-keto acids were synthesized from Acetophenone derivatives since they are inexpensive and are easily available. Keto acids act as acylating agents to deliver a carbonyl group into organic molecules via the decarboxylative coupling. Decarboxylative cross-coupling of α-keto acids has been established as a promising method of introducing a carbonyl group into a wide range of chemical compounds. In terms of mechanism, two possible reaction pathways involving an acyl metal species (RCO-M) or a free acyl radical intermediate (RCO•) are proposed for the decarboxylation process.en_US
dc.language.isoenen_US
dc.publisherIIT Roorkeeen_US
dc.titleSynthesis of aryl α-keto acids by oxidation of aryl ketonesen_US
dc.typeDissertationsen_US
Appears in Collections:MASTERS' THESES (Chemistry)

Files in This Item:
File Description SizeFormat 
20611027_Manish Pundir.pdf2.09 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.