作者:Yiyang Luo、Xianglin Yin、Mingji Dai
DOI:10.1038/s41429-019-0145-4
日期:2019.6
closing metathesis to build the corresponding macrocycle. In continuation of our efforts in developing novel carbonylation reactions to facilitate natural product total synthesis, we report herein a total synthesis of trans-resorcylide (1) featuring a palladium-catalyzed macrocyclic Stille carbonylation to build its 12-membered macrocycle.
间苯二酚大环内酯类是重要的天然产物,具有广泛的显着生物活性。到目前为止,大多数报道的间苯二酚大环内酯合成都使用大环内酯化或闭环易位来构建相应的大环。在继续努力开发新颖的羰基化反应以促进天然产物的全面合成方面,我们在此报告了以钯催化的大环Stille羰基化为特征的反式-间苯二酚(1)的全合成,以构建其十二元大环。