对映选择合成
立体中心
化学选择性
苯并呋喃
磷酰胺
化学
组合化学
位阻效应
亲核细胞
吲哚试验
配体(生物化学)
偶联反应
密度泛函理论
立体异构
立体化学
反应条件
反应机理
铃木反应
联轴节(管道)
功能群
作者
Lei Wang,Shuaijie Wu,Wenyu Zhang,Shuting Zhang,Jieya Dong,Weiming Hu,Chengcheng Zhou,Liuzhou Gao,LIEJIN ZHOU,Junliang Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-01-09
卷期号:12 (2): eaec1048-eaec1048
标识
DOI:10.1126/sciadv.aec1048
摘要
A highly efficient palladium-catalyzed enantioselective aza-Heck-catalyzed cyclization coupling reaction of alkyne-tethered oxygen- and nitrogen-centered nucleophiles is reported. This protocol enables versatile access to chiral isoindolinone-linked benzofuran and indole bis-heterocyclic derivatives bearing a quaternary stereogenic center in good yields with high enantioselectivities. A sterically demanding, electron-rich (S)-(+)-1,1'-Bi-2-naphthol (BINOL)-derived phosphoramidite ligand provides excellent control over both chemoselectivity and enantioselectivity. Density functional theory calculations were used to elucidate the reaction mechanism and the origin of enantioselectivity. Moreover, these bis-heterocycles exhibited promising antimicrobial activity.
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