Title of article
A ring-closing metathesis route to 7-membered aza-heteroannulated sugars
Author/Authors
Dominic M. Laventine، نويسنده , , Dominic M. and Jenkins، نويسنده , , Paul R. and Cullis، نويسنده , , Paul M.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
2295
To page
2298
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.
Keywords
Pyrrolidines , Amino sugars , Carbohydrate annulation , ring-closing metathesis
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1845237
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