Electrochemical Oxidative Addition of Nucleophiles on 2-Arylindoles: Synthesis of C2-Heteroquaternary Indolin-3-ones

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2024-09-12T04:19:25Z	-
dc.date.available	2024-09-12T04:19:25Z	-
dc.date.issued	2022-11	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acs.joc.2c01734	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15544	-
dc.description.abstract	An electrochemical method has been developed to synthesize 2,2-disubstituted indolin-3-ones under mild conditions. A series of nucleophiles have been added to the 2-arylindole-3-ones, generated in situ under metal-free electrochemical oxidative dearomatization of 2-arylindoles, to afford 2,2-disubstituted 3-carbonyl indoles with heteroquaternary centers in 57–79% yields.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	Electrodes	en_US
dc.subject	Fossil fuels	en_US
dc.subject	Indoles	en_US
dc.subject	Substitution reactions	en_US
dc.title	Electrochemical Oxidative Addition of Nucleophiles on 2-Arylindoles: Synthesis of C2-Heteroquaternary Indolin-3-ones	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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