Artículo
Easy Access to Configurationally Controlled C-Glycofuranoside-Based Building Blocks by Means of Formyl C-Glycofuranosides
Autor/es | Vera-Ayoso, Yolanda
Borrachero Moya, Pastora Cabrera Escribano, Francisca Gómez Guillén, Manuel Caner, Joaquín Farrás, Jaume |
Departamento | Universidad de Sevilla. Departamento de Química orgánica |
Fecha de publicación | 2010 |
Fecha de depósito | 2018-02-12 |
Publicado en |
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Resumen | 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. |
Agencias financiadoras | European Commission (EC) Junta de Andalucía |
Cita | 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. |
Ficheros | Tamaño | Formato | Ver | Descripción |
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Easy access.pdf | 119.1Kb | [PDF] | Ver/ | |