| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284927 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
The first enantioselective synthesis of (+)-dumetorine is described by ring-rearrangement reaction in a concise synthesis, using only the cheap, commercially available Grubbs I catalyst in the key step.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anke Rückert, Prashant H. Deshmukh, Siegfried Blechert,