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Synthesis 2015; 47(08): 1109-1116
DOI: 10.1055/s-0034-1380131
DOI: 10.1055/s-0034-1380131
paper
Synthesis of Pyrido[2,3-c]coumarin Derivatives by an Intramolecular Povarov Reaction
Further Information
Publication History
Received: 07 July 2014
Accepted after revision: 05 January 2015
Publication Date:
11 February 2015 (online)
Abstract
Fused pyrido[2,3-c]coumarin derivatives were prepared by an intramolecular Povarov reaction of 2-(propagyloxy)benzaldehydes with 3-aminocoumarins in the presence of 10 mol% of triflic acid as a catalyst in refluxing acetonitrile. Among the advantages of this protocol are shorter reaction times, good yields, and the absence of the need for aqueous workup and chromatographic separation.
Key words
heterocycles - pyridines - coumarins - fused-ring systems - Diels–Alder reactions - cyclizations - catalysisSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1380131.
- Supporting Information
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