| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274875 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
A general synthesis of quinolinones and benzothiazine 1,1-dioxides is presented. A series of N-phenylacrylamides and N-phenylethylenesulfonamides were studied for their ability to undergo ring closing methathesis to yield the corresponding quinolinones and benzothiazine 1,1-dioxides, respectively. The reactions are general in scope and represents a mild method for the preparation of these heterocycles.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Joannie Minville, Jason Poulin, Claude Dufresne, Claudio F. Sturino,