Please use this identifier to cite or link to this item: http://localhost:8081/jspui/handle/123456789/21456
Title: Synthesis of aryl α-keto acids by oxidation of aryl ketones
Authors: Pundir, Manish
Issue Date: Apr-2022
Publisher: IIT Roorkee
Abstract: This 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.
URI: http://localhost:8081/jspui/handle/123456789/21456
Research Supervisor/ Guide: Sharma, Anuj
metadata.dc.type: Dissertations
Appears in Collections:MASTERS' THESES (Chemistry)

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