Repositorio de producción científica de la Universidad de Sevilla

A novel approach to the synthesis of N-substituted 1-C-aminomethyl glycofuranosides

 

Advanced Search
 
Opened Access A novel approach to the synthesis of N-substituted 1-C-aminomethyl glycofuranosides
Cites

Show item statistics
Icon
Export to
Author: Vera-Ayoso, Yolanda
Borrachero Moya, Pastora
Cabrera Escribano, Francisca
Gómez Guillén, Manuel
Vogel, Pierre
Department: Universidad de Sevilla. Departamento de Química Orgánica
Date: 2006
Published in: Synlett, 1, 45-48.
Document type: Article
Abstract: Reductive amination of formyl C-glycofuranosides, easily available from hexose-derived equatorial-2-OH-glycopyranosides by DAST-promoted ring contraction, afforded N-substituted 1-C-aminomethyl glycofuranosides in most cases in high yield.
Cite: Vera-Ayoso, Y., Borrachero Moya, P., Cabrera Escribano, F., Gómez Guillén, M. y Vogel, P. (2006). A novel approach to the synthesis of N-substituted 1-C-aminomethyl glycofuranosides. Synlett, 1, 45-48.
Size: 83.34Kb
Format: PDF

URI: https://hdl.handle.net/11441/70419

DOI: 10.1055/s-2005-922762

See editor´s version

This work is under a Creative Commons License: 
Attribution-NonCommercial-NoDerivatives 4.0 Internacional

This item appears in the following Collection(s)