Issue 12, 2015

Regioselective Csp2–H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides

Abstract

A regioselective Csp2–H dual functionalization of indoles, which underlies bromo-amination via the 1,3-migration of imide groups on indolyl(phenyl)iodonium imides as novel imide-combined hypervalent iodines(III), has been developed to provide 2-bis(sulfonyl)amino-3-bromo-indoles under the metal-free conditions.

Graphical abstract: Regioselective Csp2–H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides

Supplementary files

Article information

Article type
Communication
Submitted
14 Nov 2014
Accepted
15 Dec 2014
First published
17 Dec 2014

Chem. Commun., 2015,51, 2273-2276

Regioselective Csp2–H dual functionalization of indoles using hypervalent iodine(III): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides

K. Moriyama, K. Ishida and H. Togo, Chem. Commun., 2015, 51, 2273 DOI: 10.1039/C4CC09077B

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