A Direct Access to 7-Aminoindoles via Iridium-Catalyzed Mild C-H Amidation of N-Pivaloylindoles with Organic Azides

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Ir(III)-catalyzed regioselective direct C-7 amidation of indoles in reaction with organic azides has been developed. While its efficiency was varied by the choice of N-directing groups, N-pivaloylindoles were most effective in undergoing the desired amidation at room temperature over a broad range of substrates. The reaction was scalable, and deprotection of the chelation group was also facile
Publisher
AMER CHEMICAL SOC
Issue Date
2016-04
Language
English
Article Type
Article
Keywords

BOND-FORMING REACTIONS; SULFONYL AZIDES; ARYL AZIDES; NITROGEN-SOURCE; ACTIVATION; INDOLES; AMINATION; FUNCTIONALIZATION; ARYLATION; HETEROCYCLES

Citation

ORGANIC LETTERS, v.18, no.8, pp.1892 - 1895

ISSN
1523-7060
DOI
10.1021/acs.orglett.6b00662
URI
http://hdl.handle.net/10203/209110
Appears in Collection
CH-Journal Papers(저널논문)
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