Abstract
A simple and alternative route to a versatile N-acetyl glucosamine disaccharide building block was developed, possessing a free 3-hydroxyl group. In this strategy, the 2,2,2-trichloro-ethoxy carbonyl (Troc) group was used as an amino-and 3-hydroxyl-protecting group.
Original language | English |
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Pages (from-to) | 90-100 |
Number of pages | 11 |
Journal | Arkivoc |
Volume | 2012 |
Issue number | 6 |
DOIs | |
Publication status | Published - 5 Feb 2012 |
Keywords
- Glucosamine
- Glycosylation
- N-acetyl glucosamine
- Trichloro-ethoxycarbonyl group