Issue 87, 2013

Heteroannulation of arynes with N-aryl-α-aminoketones for the synthesis of unsymmetrical N-aryl-2,3-disubstituted indoles: an aryne twist of Bischler–Möhlau indole synthesis

Abstract

Reaction of 2-(trimethylsilyl)aryl triflates 1 with N-aryl-α-amino ketones 2 afforded N-aryl-2,3-disubstituted indoles in good to excellent yields with complete control of the substitution patterns. This methodology allowed for the first time a one-step synthesis of unsymmetrical 2,3-dialkyl substituted indoles in a regiospecific manner.

Graphical abstract: Heteroannulation of arynes with N-aryl-α-aminoketones for the synthesis of unsymmetrical N-aryl-2,3-disubstituted indoles: an aryne twist of Bischler–Möhlau indole synthesis

Supplementary files

Article information

Article type
Communication
Submitted
19 Aug 2013
Accepted
05 Sep 2013
First published
10 Sep 2013

Chem. Commun., 2013,49, 10284-10286

Heteroannulation of arynes with N-aryl-α-aminoketones for the synthesis of unsymmetrical N-aryl-2,3-disubstituted indoles: an aryne twist of Bischler–Möhlau indole synthesis

A. Bunescu, C. Piemontesi, Q. Wang and J. Zhu, Chem. Commun., 2013, 49, 10284 DOI: 10.1039/C3CC46361C

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