立体中心
奥西多尔
化学
对映选择合成
磷酰胺
筑地反应
烯丙基重排
芳基
立体化学
配体(生物化学)
钯
组合化学
催化作用
有机化学
烷基
寡核苷酸
受体
DNA
生物化学
作者
Junhao Shen,Sheng‐Suo Zhou,Bailin Wang,Wenkai Liu,Zheng Wang,Xing‐Wang Wang
标识
DOI:10.1002/adsc.202201404
摘要
Abstract A Pd‐catalyzed enantioselective linear‐allylic alkylation of vinyl benzoxazinanones with a series of 3‐substituted oxindoles was reported in the presence of a chiral oxamide‐phosphine ligand (COAP−Bn) under mild reaction conditions. A series of optically active multifunctional 3,3′‐disubstituted oxindole derivatives bearing a quaternary stereogenic center and a linear aryl amino side chain were respectively obtained in 55–98% yields with 96–99% ee for 3‐(hetero)aryl substituted oxindoles. The developed protocol demonstrates that the COAP ligands could serve as a privileged chiral ligand to construct diverse chiral 3,3‐disubstituted oxindole compounds with various quaternary stereogenic centers, such as aza ‐, thio ‐ or all‐carbon quaternary stereogenic centers. The salient features of the method include broad substrate scope, N ‐protecting group free, base‐free, and high regio‐ and enantioselectivity. magnified image
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