化学
吡咯烷
立体选择性
糖苷水解酶
立体化学
亚氨基糖
复分解
会聚合成
丝氨酸
组合化学
有机化学
酶
聚合
催化作用
聚合物
作者
Celia Ribes,Eva Falomir,Juan Murga,Miguel Cardá,J. Alberto Marco
摘要
The first syntheses of the polyhydroxylated alkaloids (iminosugars) broussonetines D and M, glycosidase inhibitors of the pyrrolidine class, have been performed in a convergent, stereocontrolled way from D-serine as the chiral starting material. A cross metathesis step was one key feature of the synthesis. The versatility of the synthetic concept chosen permits the access to many members of this compound family, both natural ones and analogues thereof.
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