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

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dc.contributor.author Kumar, Anil
dc.contributor.author Kumar, Dalip
dc.date.accessioned 2021-10-14T13:12:27Z
dc.date.available 2021-10-14T13:12:27Z
dc.date.issued 2017
dc.identifier.uri https://pubs.acs.org/doi/abs/10.1021/acs.orglett.7b00617
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2836
dc.description.abstract Gold(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.iso en en_US
dc.publisher ACS en_US
dc.subject Chemistry en_US
dc.subject Indoles en_US
dc.subject Sulfides en_US
dc.subject Hydrocarbons en_US
dc.title Au-Catalyzed Synthesis of Thiopyrano[2,3-b]indoles Featuring Tandem Rearrangement and Hydroarylation en_US
dc.type Article en_US


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