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Synthesis 2017; 49(18): 4163-4172
DOI: 10.1055/s-0036-1589016
DOI: 10.1055/s-0036-1589016
special topic
2-(Aminomethyl)-3-arylindoles from 3-(o-Trifluoroacetamidoaryl)-1-propargylic Alcohols, Aryl Halides, and Amines: A Domino Palladium-Catalyzed Three-Component Approach
Further Information
Publication History
Received: 13 March 2017
Accepted after revision: 04 April 2017
Publication Date:
28 April 2017 (online)
Published as part of the Special Topic Modern Cyclization Strategies in Synthesis
Abstract
A simple, straightforward palladium-catalyzed approach to 2-(aminomethyl)-3-arylindoles from 3-(o-trifluoroacetamidoaryl)-1-propargylic alcohols, amines, and aryl iodides has been developed.
Key words
2-(aminomethyl)indoles - palladium - domino reaction - multicomponent reaction - cyclization - 3-(o-trifluoroacetamidoaryl)-1-propargylic alcoholsSupporting Information
- Supporting information for this article is available online at https://doi.org /10.1055/s-0036-1589016.
- Supporting Information
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For selected references, see:
For selected references, see:
For reviews, see:
For related acyl group migrations, see, for example:
For selected references on direct palladium-catalyzed C-3 arylation of indoles, see: