Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5229420 | Tetrahedron | 2007 | 10 Pages |
Abstract
Two enantioselective formal syntheses of (â)-swainsonine have been achieved from l-proline by using an enantioselective ring enlargement of a substituted prolinol as the key step. The more efficient synthesis has been achieved in 14 steps with an overall yield of 14%.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ingrid Déchamps, Domingo Gomez Pardo, Janine Cossy,