Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
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.
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| Format: | article |
| Language: | eng |
| Published: |
2020
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| Online Access: | http://hdl.handle.net/10362/92206 |
| Country: | Portugal |
| Oai: | oai:run.unl.pt:10362/92206 |
| Summary: | 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. |
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