Dominic M. Laventine, P. R. Jenkins, P. Cullis
Mar 28, 2005
Citations
0
Influential Citations
14
Citations
Journal
Tetrahedron Letters
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 has also been employed to afford a tetrahydroxylated azepane carbohydrate derivative with potential biological activity.