立体中心
化学
对映选择合成
氨基酯
立体化学
配体(生物化学)
组合化学
催化作用
糖苷键
四氢呋喃
立体选择性
氨基酸
不对称诱导
不对称碳
手性(物理)
钴
均分解
烯烃
作者
Tingting Xia,Hongrui Feng,Qihang Cao,Xijian Yang,Xianqing Wu,Wei‐Hong Zhu,Jingping Qu,Yuehua Chen
标识
DOI:10.1002/anie.202521583
摘要
Abstract Chiral oxygen‐containing heterocycles, particularly tetrahydrofuran scaffolds are pivotal structures found in numerous bioactive molecules. Among them, furanoses constitute a highly important class. While C‐glycosylation with furanosyl donors offers a promising route to access these frameworks, methods for simultaneously constructing multiple stereogenic centers remain unknown. Herein, we report a synergistic photoredox/cobalt‐catalyzed enantioselective radical addition strategy to imines that employs bench‐stable furanosyl 1,4‐dihydropyridines (DHPs) as the radical precursors. This redox‐neutral protocol directly forges C‐glycosidic bonds at the challenging non‐anomeric position while concurrently establishing a new tetrasubstituted carbon stereocenter. The chiral cobalt catalyst effectively governs the stereochemistry of both the glycosidic bond and the new tetrasubstituted center, as evidenced by ligand control experiments. Furthermore, the method is generalizable to simple alkyl‐substituted DHPs, providing a versatile and complementary approach to synthesize amino esters and C‐glycosides with multiple stereogenic centers.
科研通智能强力驱动
Strongly Powered by AbleSci AI