Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2021-10-27T04:27:18Z	-
dc.date.available	2021-10-27T04:27:18Z	-
dc.date.issued	2019	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra04741g	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3161	-
dc.description.abstract	An efficient protocol for the synthesis of 2,2-disubstituted indolin-3-ones under mild conditions has been developed. This reaction involves the copper-catalyzed in situ oxidative de-aromatization of 2-arylindoles to indol-3-one, followed by self-dimerization as well as cross-addition with indoles under mild conditions. The result generates a wide variety of C2-tetrasubstituted indolin-3-ones with good to high yields (62–82%).	en_US
dc.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Chemistry	en_US
dc.subject	C2-tetrasubstituted	en_US
dc.subject	Indolin-3-ones	en_US
dc.subject	Cu-catalyzed	en_US
dc.title	Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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