Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5278991 | Tetrahedron Letters | 2009 | 6 Pages |
Abstract
An efficient, green, room temperature process for the stereoselective synthesis of β-amido ketones employing a one-pot multi-component reaction of aromatic aldehydes, α-substituted or α-unsubstituted ketones, an acid chloride, and a nitrile in presence of catalytic amount of Selectfluor⢠is described. The process offers advantages such as high anti-selectivity, shorter reaction time, energy efficiency, and simple work-up.
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Authors
V.S. Shinu, B. Sheeja, E. Purushothaman, D. Bahulayan,