A double diastereoselective michael-type addition as an entry to conformationally restricted Tn antigen mimics

  1. Aydillo, C. 1
  2. Navo, C.D. 1
  3. Busto, J.H. 1
  4. Corzana, F. 1
  5. Zurbano, M.M. 1
  6. Avenoza, A. 1
  7. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Revista:
Journal of Organic Chemistry

ISSN: 0022-3263

Año de publicación: 2013

Volumen: 78

Número: 21

Páginas: 10968-10977

Tipo: Artículo

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DOI: 10.1021/JO4019396 SCOPUS: 2-s2.0-84887108285 WoS: WOS:000326615300041 GOOGLE SCHOLAR

Otras publicaciones en: Journal of Organic Chemistry

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Diseño racional de glicopéptidos con aplicaciones en Química Biológica

2013/00007/001

Resumen

A totally stereocontrolled C-Michael addition of serine-equivalent C-nucleophiles to tri-O-benzyl-2-nitro-d-galactal was used as the key step to synthesize several pyrano[3,2-b]pyrrole structures. These scaffolds could be regarded as conformationally restricted Tn antigen mimics, as we have demonstrated by biological assays. The pyranose rings retain their 4C1 chair conformation, as shown by molecular modeling and NMR spectroscopy. The expected bioactivity was established by a competition-tailored enzyme-linked lectin assay using both soybean and Vicia villosa agglutinins as model lectins. The facile described synthetic route and the strategic combination of computational and experimental techniques to reveal conformational features and bioactivity demonstrate the prepared glycomimics to be promising candidates for further exploitation of this scaffold to give glycans for lectin blocking and vaccination. © 2013 American Chemical Society.