| dc.contributor.author | Kumar, Anil | |
| dc.date.accessioned | 2021-10-17T13:56:47Z | |
| dc.date.available | 2021-10-17T13:56:47Z | |
| dc.date.issued | 2020-04-20 | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/jo5025943 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2863 | |
| dc.description.abstract | An efficient methodology for the synthesis of indole-fused dihydrothiopyrans has been developed from indoline-2-thiones. The protocol involves the synthesis of conjugated ene-yne-substituted indole-sulfides, a gold(III)-catalyzed rearrangement of the ene-yne side chain followed by intramolecular hydroarylation via C3–H functionalization of the indole core. This new synthesis of functionalized tricyclic indole derivatives through sequential rearrangements is quite general in nature | 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 | Hydrocarbons | en_US |
| dc.subject | Aromatic compounds | en_US |
| dc.title | NEXT Access to Substituted Dihydrothiopyrano[2,3-b]indoles via Sequential Rearrangements During S-Alkylation and Au-Catalyzed Hydroarylation on Indoline-2-thiones | en_US |
| dc.type | Article | en_US |
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