Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3165
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar, Dalip | - |
dc.contributor.author | Kumar, Indresh | - |
dc.date.accessioned | 2021-10-27T04:27:29Z | - |
dc.date.available | 2021-10-27T04:27:29Z | - |
dc.date.issued | 2017 | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2017/ob/c7ob00940b | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3165 | - |
dc.description.abstract | Regioselective construction of crucial C–N and C–O bonds leading to N-arylquinolones and aryloxyquinolines has been accomplished by employing easily accessible diaryliodonium salts and quinolones in water under metal- and ligand-free conditions. This operationally simple strategy is significant due to mild reaction conditions, high product yields, recyclability of released iodoarenes and scalability to the gram level. The practical utility of the developed protocol was proved by the arylation of medicinally important heterocycles like acridin-9(10H)-one, 3-methylquinoxalin-2(1H)-one and 1H-benzo[d]imidazol-2(3H)-one. | en_US |
dc.language.iso | en | en_US |
dc.publisher | RSC | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Synthesis | en_US |
dc.subject | N-arylquinolones | en_US |
dc.subject | Aryloxyquinolines | en_US |
dc.title | Metal-free regioselective formation of C–N and C–O bonds with the utilization of diaryliodonium salts in water: facile synthesis of N-arylquinolones and aryloxyquinolines | 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.