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

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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