Au-Catalyzed Synthesis of Thiopyrano[2,3-b]indoles Featuring Tandem Rearrangement and Hydroarylation

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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.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.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.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

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