| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217535 | Tetrahedron | 2013 | 5 Pages |
Abstract
2-Chloro-N-ethoxycarbonylmethylpyridinium bromide reacts with substituted acetonitriles in two steps; the initially formed pyridine anhydro baseses undergo further ring closure to 2-amino-3-ethoxycarbonylindolizines.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
