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Synthesis 2013; 45(5): 633-638
DOI: 10.1055/s-0032-1318112
DOI: 10.1055/s-0032-1318112
paper
Palladium-Catalyzed Cross-Coupling of 1,4-Disubstituted 5-Iodo-1,2,3-triazoles with Organotin Reagents
Further Information
Publication History
Received: 31 October 2012
Accepted after revision: 27 December 2012
Publication Date:
01 February 2013 (online)
Abstract
In a new synthetic approach for building systems bearing a 1,2,3-triazole moiety, we report here the first Stille cross-coupling reaction of 1,4-disubstituted 5-iodo-1,2,3-triazoles with a range of stannyl derivatives to give the corresponding 5-vinyl-1,2,3-triazoles.
Key words
1,2,3-triazoles - click chemistry - palladium catalyst - Stille cross-coupling reaction - vinyltin reagentsSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis. Included are copies of 1H and 13C NMR spectra of compounds 3 and 5.
- Supporting Information
-
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For 1,2,3-triazoles used for biotechnology applications see:
For 1,2,3-triazoles applied to materials sciences see:
For general information on 1,2,3-triazoles see:
For palladium-catalyzed reactions see:
For palladium-free reactions see: