Synthesis of a New Conformationally Constrained Glycoamino Acid Building Block

  1. Avenoza, A. 1
  2. Peregrina, J.M. 1
  3. San Martín, E. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Journal:
Tetrahedron Letters

ISSN: 0040-4039

Year of publication: 2003

Volume: 44

Issue: 34

Pages: 6413-6416

Type: Article

DOI: 10.1016/S0040-4039(03)01586-7 SCOPUS: 2-s2.0-0042197276 WoS: WOS:000184618600012 GOOGLE SCHOLAR

More publications in: Tetrahedron Letters

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Abstract

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.