| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274464 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
New 2,3-dihydropyrrolopyridinones were conveniently prepared by trapping lithiated pyridine carboxamides with highly reactive formimines. In this Letter, we report that a wide range of N-functionalised compounds can be synthesised in one step by this process, allowing the presence of ethers, acetals or ester moieties.
Graphical abstractNew 2,3-dihydropyrrolopyridinones were prepared by trapping lithiated pyridine carboxamides with highly reactive formimines. This method allowed a wide range of N-functionalised compounds including ethers, acetals or ester moieties.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Emilie Prieur, Rabah Azzouz, Geoffrey Deguest, Corinne Fruit, Laurent Bischoff, Francis Marsais,