Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274947 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
2H-Pyran-2-ones are useful precursors for the synthesis of various aromatic and heterocyclic compounds. In this Letter, we describe substituent-controlled direct access to functionalized 4-(2-oxo-1,2-diarylethyl)-5,6-diaryl-pyran-2-ones by stirring a mixture of 3-cyano-5,6-diaryl-2H-pyran-2-ones and functionalized deoxybenzoins through an unusual decyanation reaction. Under similar reaction conditions, the reactions of 3-carbomethoxy-5,6-diaryl-2H-pyran-2-ones with either substituted acetophenones or deoxybenzoins led to the synthesis of pyrano[3,4-c]pyran-1,8-diones in excellent yields.
Related Topics
Physical Sciences and Engineering
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Authors
Fateh V. Singh, Manish Dixit, Sumit Chaurasia, Resmi Raghunandan, Prakas R. Maulik, Atul Goel,