阿托品
化学
电泳剂
亲核细胞
组合化学
分子内力
对映选择合成
胺气处理
醌
对映体药物
芳基
催化作用
有机化学
立体化学
烷基
作者
Chang‐Qiu Guo,Chuan‐Jun Lu,Li‐Wen Zhan,Peng Zhang,Qi Xu,Jia Feng,Jianrong Gao
标识
DOI:10.1002/anie.202212846
摘要
Diarylamines and related scaffolds are ubiquitous atropisomeric chemotypes in biologically active natural products. However, the catalytic asymmetric synthesis of these axially chiral compounds remains largely unexplored. Herein, we report that a BINOL-derived chiral phosphoric acid (CPA) successfully catalyzed the atroposelective coupling of quinone esters and anilines through direct C-N bond formation to afford N-aryl quinone atropisomers with an unprecedented intramolecular N-H-O hydrogen bond within a six-membered ring in good yields and enantioselectivities with the quinone ester as both the electrophile and the oxidant. A gram-scale experiment demonstrated the utility of this synthetic protocol. Moreover, this methodology provides a platform for the synthesis of structurally diverse secondary amine atropisomers by nucleophilic addition.
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