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Synthesis 2017; 49(06): 1356-1370
DOI: 10.1055/s-0036-1588655
DOI: 10.1055/s-0036-1588655
paper
Synthesis of Tricyclic Isoxazoles via Sequential [3+2] Dipolar Cycloaddition and Palladium-Catalyzed Intramolecular Arylation Reactions
Further Information
Publication History
Received: 20 August 2016
Accepted after revision: 27 October 2016
Publication Date:
01 December 2016 (online)
Abstract
An efficient synthetic route to tricyclic isoxazoles via sequential copper-catalyzed 1,3-dipolar cycloaddition and palladium-catalyzed intramolecular arylation of isoxazoles is described. Based on these reactions, a convenient one-pot synthesis of the tricyclic isoxazoles from terminal alkyne and hydroximoyl chlorides by using a cascade process was also developed.
Key words
isoxazoles - C–H activation - 1,3-dipolar cycloaddition - intramolecular arylation - tandem processesSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0036-1588655.
- Supporting Information
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