化学
电泳剂
催化作用
铬
芳基
硝基
药物化学
电子转移
组合化学
有机化学
烷基
作者
Seiji Shirakawa,Kenichiro Yamamoto,Keiji Maruoka
标识
DOI:10.1002/anie.201409065
摘要
Abstract Although phase‐transfer‐catalyzed asymmetric S N Ar reactions provide unique contribution to the catalytic asymmetric α‐arylations of carbonyl compounds to produce biologically active α‐aryl carbonyl compounds, the electrophiles were limited to arenes bearing strong electron‐withdrawing groups, such as a nitro group. To overcome this limitation, we examined the asymmetric S N Ar reactions of α‐amino acid derivatives with arene chromium complexes derived from fluoroarenes, including those containing electron‐donating substituents. The arylation was efficiently promoted by binaphthyl‐modified chiral phase‐transfer catalysts to give the corresponding α,α‐disubstituted α‐amino acids containing various aromatic substituents with high enantioselectivities.
科研通智能强力驱动
Strongly Powered by AbleSci AI