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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3165
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dc.contributor.authorKumar, Dalip-
dc.contributor.authorKumar, Indresh-
dc.date.accessioned2021-10-27T04:27:29Z-
dc.date.available2021-10-27T04:27:29Z-
dc.date.issued2017-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2017/ob/c7ob00940b-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3165-
dc.description.abstractRegioselective 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.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectN-arylquinolonesen_US
dc.subjectAryloxyquinolinesen_US
dc.titleMetal-free regioselective formation of C–N and C–O bonds with the utilization of diaryliodonium salts in water: facile synthesis of N-arylquinolones and aryloxyquinolinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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