First Total Synthesis of (3R,4S)-4-Hydroxylasiodiplodin: A Facile and Stereoselective Approach
作者:Saibal Das、Sheshurao Bujaranipalli、Gyan Eppa
DOI:10.1055/s-0032-1317805
日期:——
A first total synthesis of (3R,4S)-4-hydroxylasiodiplodin is described starting from methyl acetoacetate and a commonly available carbohydrate, d -mannitol, which is regularly used in organic synthesis. The facile and stereoselective approach involves the Barbier allylation and a ring-closing metathesis as key steps.
(3R,4S)-4-hydroxylasiodiplodin 的第一个全合成描述了从乙酰乙酸甲酯和常用的碳水化合物,d-甘露醇开始,d-甘露醇经常用于有机合成。简便的立体选择性方法涉及作为关键步骤的 Barbier 烯丙基化和闭环复分解。