Issue 11, 2017

Mechanochemical indole synthesis by rhodium-catalysed oxidative coupling of acetanilides and alkynes under solventless conditions in a ball mill

Abstract

A mechanochemical indole synthesis by rhodium(III)-catalysed C–H bond functionalisation in a planetary mill has been developed. It occurs in the absence of any solvent, does not require additional heating and only needs catalytic quantities of Cu(OAc)2 in combination with dioxygen as a terminal oxidant. Accordingly, the process represents a powerful and environmentally benign alternative to the common solution-based standard protocols.

Graphical abstract: Mechanochemical indole synthesis by rhodium-catalysed oxidative coupling of acetanilides and alkynes under solventless conditions in a ball mill

Supplementary files

Article information

Article type
Communication
Submitted
15 Feb 2017
Accepted
28 Apr 2017
First published
28 Apr 2017

Green Chem., 2017,19, 2520-2523

Mechanochemical indole synthesis by rhodium-catalysed oxidative coupling of acetanilides and alkynes under solventless conditions in a ball mill

G. N. Hermann, C. L. Jung and C. Bolm, Green Chem., 2017, 19, 2520 DOI: 10.1039/C7GC00499K

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