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Synlett 2016; 27(09): 1397-1402
DOI: 10.1055/s-0035-1561566
DOI: 10.1055/s-0035-1561566
letter
Synthesis of Novel Imidazopyrrolo-Fused Isoxazole Derivatives through Acid-Mediated Intramolecular 1,3-Dipolar Cycloaddition
Further Information
Publication History
Received: 24 November 2015
Accepted after revision: 15 January 2016
Publication Date:
04 March 2016 (online)
Abstract
A facile approach to 4H-imidazo[1′,2′:1,2]pyrrolo[3,4-c]isoxazole derivatives was developed via intramolecular 1,3-dipolar cycloaddition catalyzed by p-toluenesulfonic acid. The method allows the convenient construction of novel tricyclic isoxazoles under mild reaction conditions and moderate yields.
Key words
1,3-dipolar cycloaddition - 2-nitro-1,1-ethenediamine - nitromethylene-imidazolidine - p-toluenesulfonic acid - tricyclic isoxazolesSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1561566.
- Supporting Information
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