Title | Synthesis of 1-amino-1,2,5-trideoxy-2,5-imino-D-mannitol, a novel analogue of the powerful glucosidase inhibitor 2,5-dideoxy-2,5-imino-D-mannitol, via an Amadori rearrangement of 5-azido-5-deoxy-D-glucofuranose |
Publication Type | Journal Article |
Year of Publication | 1997 |
Authors | Wrodnigg, TM, Stutz, AE, Withers, SG |
Journal | TETRAHEDRON LETTERS |
Volume | 38 |
Pagination | 5463-5466 |
Date Published | AUG 4 |
ISSN | 0040-4039 |
Abstract | By an Amadori rearrangement of easily available 5-azido-5-deoxy-D-glucofuranose with dibenzylamine and subsequent catalytic hydrogenation of the resulting 5-azido-1-dibenzylamino-1,5-dideoxy-D-fructopyranose, the new 1-amino-1,2,5-trideoxy-2,5-imino-D-mannitol was obtained in only two steps and excellent overall yield. Likewise, other amines and/or other 5-modified hexofuranoses can be used to advantage. The reported rearrangement reaction is a high yielding, convenient and apparently general entry to 1-aminodeoxyketopyranoses modified at C-5, facilitated by the ring enlargement of the aldofuranose to the ketopyranose as an additional driving force. (C) 1997 Elsevier Science Ltd. |
DOI | 10.1016/S0040-4039(97)01198-2 |
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