Artículo
Synthesis of Novel 3-Amino(Hydroxy)methyl-l-fuco-Azafagomines as Leads for Selective Inhibitors of α-l-Fucosidases
Autor/es | Moreno Clavijo, Elena
Carmona Asenjo, Ana Teresa Moreno Vargas, Antonio José Álvarez González, Eleuterio Robina Ramírez, Inmaculada |
Departamento | Universidad de Sevilla. Departamento de Química orgánica |
Fecha de publicación | 2010 |
Fecha de depósito | 2018-02-09 |
Publicado en |
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Resumen | The synthesis of 3-substituted l-fuco-azafagomines from d-lyxose is reported. They represent the first example of aza-C-glycosides having a biimino (-NH-NH-) moiety. The key step of the synthesis is the introduction of the ... The synthesis of 3-substituted l-fuco-azafagomines from d-lyxose is reported. They represent the first example of aza-C-glycosides having a biimino (-NH-NH-) moiety. The key step of the synthesis is the introduction of the hydrazine moiety by reductive hydrazination of a 1-deoxy-ketohexose with tert-butyl carbazate. Their glycosidase inhibitory properties are also reported. |
Agencias financiadoras | Ministerio de Ciencia e Innovación (MICIN). España Junta de Andalucía |
Cita | Moreno Clavijo, E., Carmona Asenjo, A.T., Moreno Vargas, A.J., Álvarez, E. y Robina Ramírez, I. (2010). Synthesis of Novel 3-Amino(Hydroxy)methyl-l-fuco-Azafagomines as Leads for Selective Inhibitors of α-l-Fucosidases. Synlett, 9, 1367-1370. |
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