作者:Berit Schwesinger、Reinhard Schwesinger、Horst Prinzbach
DOI:10.1016/s0040-4039(01)90091-7
日期:1984.1
A convenient synthesis of methyl α-D-purpurosaminide C has been developed starting from dimeric acrolein (25–30 % overall yield of each enantiomer). Key steps are the efficient separation of intermediate diastereomeric amines and the stereospecific reduction of 2-oximino-α-hexopyranosides.
从二聚丙烯醛(每种对映异构体的总产率为25%到30%)开始,已经开发了一种方便的甲基α-D-purpurosaminideC合成方法。关键步骤是有效分离中间非对映异构胺和2-氧亚氨基-α-己吡喃糖苷的立体定向还原。