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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/123456789/2846
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-14T13:13:21Z-
dc.date.available2021-10-14T13:13:21Z-
dc.date.issued2016-
dc.identifier.urihttps://pubs.rsc.org/en/Content/ArticleLanding/OB/2016/C6OB00117C-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2846-
dc.description.abstractA simple and efficient method for the synthesis of biologically relevant 5H-benzo[4,5][1,3]thiazino[3,2-a]indoles and 5,7-dihydroisothiochromeno[3,4-b]indoles has been developed via intramolecular copper catalysed Ullmann-type C–N coupling and palladium catalysed direct arylation from the corresponding precursors 2-(2-bromobenzylthio)-1H-indole and 2-(2-bromobenzylthio)-1-methyl-1H-indole, respectively, in good to excellent yields.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectCopper-catalyseden_US
dc.titleSynthesis of indole-annulated sulfur heterocycles using copper-catalysed C–N coupling and palladium-catalysed direct arylationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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