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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/2836
Title: Au-Catalyzed Synthesis of Thiopyrano[2,3-b]indoles Featuring Tandem Rearrangement and Hydroarylation
Authors: Kumar, Anil
Kumar, Dalip
Keywords: Chemistry
Indoles
Sulfides
Hydrocarbons
Issue Date: 2017
Publisher: ACS
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.
URI: https://pubs.acs.org/doi/abs/10.1021/acs.orglett.7b00617
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2836
Appears in Collections:Department of Chemistry

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