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) |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 20611027_Manish Pundir.pdf | 2.09 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
