Lanke, Veeranjaneyulu and Prabhu, Kandikere Ramaiah (2017) Iridium(III) catalyzed regioselective amidation of indoles at the C4-position using weak coordinating groups. In: CHEMICAL COMMUNICATIONS, 53 (37). pp. 5117-5120.
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Abstract
The C4-aminated indole scaffold is frequently encountered in several natural products and biologically active compounds. Herein we disclose a simple and short synthetic route for the amidation of indoles at the C4 position by employing an aldehyde as a directing group and Ir(III) as a catalyst. This strategy offers high selectivity for the C4-amidation of unprotected and protected indoles. A simple deprotection of the tosyl group leads to the formation of C4-amino indole derivatives, which are useful synthons for synthesizing natural products in the teleocidin family.
Item Type: | Journal Article |
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Publication: | CHEMICAL COMMUNICATIONS |
Additional Information: | Copy right for this article belongs to the ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 10 Jun 2017 04:39 |
Last Modified: | 10 Jun 2017 04:39 |
URI: | http://eprints.iisc.ac.in/id/eprint/57161 |
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