| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276891 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
1-Deoxynojirimycin (DNJ) and 1-deoxymannojirimycin (DMJ) were synthesized through a concise and practicable pathway. A strategy of using carbohydrate derivatives bearing two leaving groups in the preparation of azasugars by di-N-alkylation of amines was developed. The strategy involved the selective partial protection of dibromo alditols.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xuezheng Song, Rawle I. Hollingsworth,