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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pundir, Manish | - |
| dc.date.accessioned | 2026-09-17T10:52:46Z | - |
| dc.date.available | 2026-09-17T10:52:46Z | - |
| dc.date.issued | 2022-04 | - |
| dc.identifier.uri | http://localhost:8081/jspui/handle/123456789/21456 | - |
| dc.guide | Sharma, Anuj | en_US |
| dc.description.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. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | IIT Roorkee | en_US |
| dc.title | Synthesis of aryl α-keto acids by oxidation of aryl ketones | en_US |
| dc.type | Dissertations | en_US |
| 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 |
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