作者:Hans Rudolf Pfaendler、Volker Weimar
DOI:10.1055/s-1996-4390
日期:1996.11
Racemic C12-ethanolamine plasmalogen 5b was prepared in high yield. The amino group was generated by selective reaction of azide 4b with polymeric triphenylphosphine followed by mild hydrolysis of the intermediate phosphine imine. A novel universal phosphorylation reagent 2-azidoethyl dichlorophosphate (7) was used.
外消旋 C12-乙醇胺质卤素 5b 是以高产率制备的。通过叠氮化物 4b 与聚合三苯基膦的选择性反应生成氨基,然后对中间膦亚胺进行温和水解。使用了一种新型通用磷酸化试剂 2-azidoethyl dichlorophosphate (7)。