| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5292955 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Azepane rings have been constructed diastereoselectively upon a carbohydrate derivative utilising reductive amination and RCM. The stereochemistry of the ring junctions was confirmed by X-ray crystallography and NMR. Diastereoselective dihydroxylation gave a tetrahydroxylated azepane carbohydrate derivative.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dominic M. Laventine, Paul R. Jenkins, Paul M. Cullis,