Merchán F L, Merino P, Tejero T
Departamento de Química Orgánica, ICMA, Universidad de Zaragoza, Spain.
Glycoconj J. 1997 Jun;14(4):497-9. doi: 10.1023/a:1018559720428.
A new procedure for the introduction of a nitrogen atom into the anomeric centre leading to glycosylamines is described. The new reaction consisting of the condensation of a furanose with a hydroxylamine in the presence of a Lewis acid occurs with a complete degree of diastereoselectivity.
描述了一种将氮原子引入异头中心以生成糖胺的新方法。新反应是在路易斯酸存在下,呋喃糖与羟胺缩合,反应具有完全的非对映选择性。