Selective protecting group manipulations on the 1-deoxynojirimycin scaffold
E Danieli, J Lalot, PV Murphy
Index: Danieli, Elisa; Lalot, Jerome; Murphy, Paul V. Tetrahedron, 2007 , vol. 63, # 29 p. 6827 - 6834
Full Text: HTML
Citation Number: 15
Abstract
Iminosugars are inhibitors of glycoprocessing and are of interest as scaffolds for medicinal chemistry, as their successful application as peptide mimetics has shown. The synthesis of novel peptidomimetics based on 1-deoxynojirimycin (DNJ) requires practical strategies that allow introduction of amino acid side chains or pharmacophore groups at each of its hydroxyl groups or to the nitrogen atom. This paper describes one approach towards ...
Related Articles:
Quantifying electronic effects of common carbohydrate protecting groups in a piperidine model system
[Heuckendorff, Mads; Pedersen, Christian M.; Bols, Mikael Chemistry - A European Journal, 2010 , vol. 16, # 47 p. 13982 - 13994]