Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2811
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar, Anil | - |
dc.date.accessioned | 2021-10-14T13:09:52Z | - |
dc.date.available | 2021-10-14T13:09:52Z | - |
dc.date.issued | 2020 | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2020/ob/d0ob01842b | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2811 | - |
dc.description.abstract | A simple and straightforward approach has been realized for the direct benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids in the presence of K2S2O8 as an oxidant. Various functional groups were tolerated on both imidazoheterocycles and arylglyoxylic acids and a wide range of C5-benzoyl-imidazoheterocycles were obtained in good to high yields (50–84%). Radical trapping experiments confirmed the involvement of the radical pathway. The developed protocol is amenable for a scale-up reaction. | en_US |
dc.language.iso | en | en_US |
dc.publisher | RSC | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Benzoylation | en_US |
dc.subject | Imidazoheterocycles | en_US |
dc.subject | Arylglyoxylic acids | en_US |
dc.title | Metal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.