Ligand-Enabled Stereoselective 尾-C(sp3)鈥揌 Fluorination: Synthesis of Unnatural Enantiopure anti-尾-Fluoro-伪-amino Acids
详细信息    查看全文
文摘
A quinoline-based ligand was shown to promote palladium-catalyzed 尾-C(sp3)鈥揌 fluorination for the first time. A range of unnatural enantiopure fluorinated 伪-amino acids were obtained through sequential 尾-C(sp3)鈥揌 arylation and subsequent stereoselective fluorination from readily available l-alanine.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700