Substrate or Solvent-Controlled PdII-Catalyzed Regioselective Arylation of Quinolin-4(1H)-ones Using Diaryliodonium Salts: Facile Access to Benzoxocine and Aaptamine Analogues

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dc.contributor.authorKumar, Dalip
dc.date.accessioned2021-10-27T04:18:38Z
dc.date.available2021-10-27T04:18:38Z
dc.date.issued2020-03-11
dc.description.abstractSubstrate or solvent controlled regioselective C3, C5, and C8 arylation of quinolin-4(1H)-ones with diaryliodonium salts have been successfully achieved in high yields (up to 96 %). These protocols are applicable to a wide range of quinolone related heterocycles and provide potential access to naturally occurring benzoxocine and aaptamine analoguesen_US
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000013
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3013
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectDiaryliodonium Saltsen_US
dc.subjectBenzoxocineen_US
dc.subjectAaptamine Analoguesen_US
dc.titleSubstrate or Solvent-Controlled PdII-Catalyzed Regioselective Arylation of Quinolin-4(1H)-ones Using Diaryliodonium Salts: Facile Access to Benzoxocine and Aaptamine Analoguesen_US
dc.typeArticleen_US

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