| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271668 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
We developed an efficient synthetic strategy of poly-substituted pyrroles via an indium-mediated Barbier type allylation from γ-ketonitriles. Initial attack of allylindium species occurred at the nitrile group selectively to form the enamine intermediate, which reacted with the ketone group intramolecularly to furnish the pyrroles.
Graphical abstractDownload full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sung Hwan Kim, Se Hee Kim, Ka Young Lee, Jae Nyoung Kim,