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 Field	Value	Language
dc.contributor.author	Kumar, Dalip	-
dc.date.accessioned	2021-10-27T04:18:38Z	-
dc.date.available	2021-10-27T04:18:38Z	-
dc.date.issued	2020-03-11	-
dc.identifier.uri	https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000013	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3013	-
dc.description.abstract	Substrate 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 analogues	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Diaryliodonium Salts	en_US
dc.subject	Benzoxocine	en_US
dc.subject	Aaptamine Analogues	en_US
dc.title	Substrate or Solvent-Controlled PdII-Catalyzed Regioselective Arylation of Quinolin-4(1H)-ones Using Diaryliodonium Salts: Facile Access to Benzoxocine and Aaptamine Analogues	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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