Article
Easy Access to Configurationally Controlled C-Glycofuranoside-Based Building Blocks by Means of Formyl C-Glycofuranosides
Author/s | Vera-Ayoso, Yolanda
Borrachero Moya, Pastora Cabrera Escribano, Francisca Gómez Guillén, Manuel Caner, Joaquín Farrás, Jaume |
Department | Universidad de Sevilla. Departamento de Química orgánica |
Publication Date | 2010 |
Deposit Date | 2018-02-12 |
Published in |
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Abstract | A general approach to enantiopure C-glycofuranoside-based hybridα/β-amino acids and nitrones, among other valuable building blocks, has been established via formyl C-glycofuranosides, easily available from hexose-derived ... A general approach to enantiopure C-glycofuranoside-based hybridα/β-amino acids and nitrones, among other valuable building blocks, has been established via formyl C-glycofuranosides, easily available from hexose-derived equatorial-2-OH-glycopyranosides by DAST-promoted ring contraction. © Georg Thieme Verlag Stuttgart New York. |
Funding agencies | European Commission (EC) Junta de Andalucía |
Citation | Vera-Ayoso, Y., Borrachero Moya, P., Cabrera Escribano, F., Gómez Guillén, M., Caner, J. y Farrás, J. (2010). Easy Access to Configurationally Controlled C-Glycofuranoside-Based Building Blocks by Means of Formyl C-Glycofuranosides. Synlett, 2, 271-275. |
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