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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/123456789/2836
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dc.contributor.authorKumar, Anil-
dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-14T13:12:27Z-
dc.date.available2021-10-14T13:12:27Z-
dc.date.issued2017-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.orglett.7b00617-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2836-
dc.description.abstractGold(III)-catalyzed synthesis of 14-π electron heteroaromatic thiopyrano[2,3-b]indole is reported using conjugated enyne tethered indole sulfides, featuring skeletal rearrangement conjoined with intramolecular hydroarylation (via C3–H functionalization of the indole core) and oxidative aromatization. Subsequent Pd-catalyzed C–C coupling resulted in a 16-π electron heteroaromatic isothiochromeno[1,8,7-bcd]indole.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectIndolesen_US
dc.subjectSulfidesen_US
dc.subjectHydrocarbonsen_US
dc.titleAu-Catalyzed Synthesis of Thiopyrano[2,3-b]indoles Featuring Tandem Rearrangement and Hydroarylationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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