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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

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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


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