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...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2003 |
| País: | España |
| Institución: | Universidad de La Rioja (UR) |
| Repositorio: | RIUR. Repositorio Institucional de la Universidad de La Rioja |
| OAI Identifier: | oai:portal.dialnet.es:doc/5bbc690cb750603269e8141b |
| Acceso en línea: | https://investigacion.unirioja.es/documentos/5bbc690cb750603269e8141b |
| Access Level: | acceso abierto |
| Palabra clave: | Amino acids and derivatives Azides Glycosidation Peptide analogues/mimetics |
| Sumario: | 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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