Synthesis of a New Conformationally Constrained Glycoamino Acid Building Block
The synthesis of a suitably protected β-D-glucopyranosyl-(S)-α-methylserine derivative - a new conformationally constrained glycosylated quaternary amino acid analogue of β-D-glucopyranosyl-L-serine - is described. This compound can be used as an attractive building block for the synthesis of new, c...
| Authors: | , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2003 |
| Country: | España |
| Institution: | Universidad de La Rioja (UR) |
| Repository: | RIUR. Repositorio Institucional de la Universidad de La Rioja |
| OAI Identifier: | oai:portal.dialnet.es:doc/5bbc690cb750603269e8141b |
| Online Access: | https://investigacion.unirioja.es/documentos/5bbc690cb750603269e8141b |
| Access Level: | Open access |
| Keyword: | Amino acids and derivatives Azides Glycosidation Peptide analogues/mimetics |
| Summary: | The synthesis of a suitably protected β-D-glucopyranosyl-(S)-α-methylserine derivative - a new conformationally constrained glycosylated quaternary amino acid analogue of β-D-glucopyranosyl-L-serine - is described. This compound can be used as an attractive building block for the synthesis of new, constrained glycopeptides. © 2003 Elsevier Ltd. All rights reserved. |
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