Disclosed are small molecule inhibitors which are useful in treating various diseases and conditions involving chymase.
Also disclosed are pharmaceutical compositions, methods of using and making the same.
Palladium-Catalyzed Site-Selective Fluorination of Unactivated C(sp<sup>3</sup>)–H Bonds
作者:Jinmin Miao、Ke Yang、Martin Kurek、Haibo Ge
DOI:10.1021/acs.orglett.5b01710
日期:2015.8.7
The transition-metal-catalyzed direct C–H bond fluorination is an attractive synthetic tool toward the preparation of organofluorines. While many methods exist for the direct sp3 C–H functionalization, site-selective fluorination of unactivated sp3 carbons remains a challenge. Direct, highly site-selective and diastereoselective fluorination of aliphatic amides via a palladium-catalyzed bidentate ligand-directed