Late stage C-H functionalization via chalcogen and pnictogen salts

被引:58
作者
Kelly, Christopher B. [1 ]
Padilla-Salinas, Rosaura [1 ]
机构
[1] Janssen Res & Dev LLC, Discovery Proc Res, 1400 McKean Rd, Spring House, PA 19477 USA
关键词
LIGHT PHOTOREDOX CATALYSIS; SINGLE-ELECTRON TRANSMETALATION; PHENYL-PYRIDINIUM CHLORIDE; PHOSPHONIUM SALTS; CARBON-CARBON; BOND FUNCTIONALIZATION; NICKEL CATALYSIS; SULFONIUM SALTS; CROSS-COUPLINGS; ION RADICALS;
D O I
10.1039/d0sc03833d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Late-stage functionalization (LSF) of heteroarenes can dramatically accelerate SAR studies by enabling the installation of functional groups that would otherwise complicate a synthetic sequence. Although heteroaryl halides and boronic esters have well-established chemistries for LSF, alternatives that enable site-selective C-H functionalization are highly attractive. Recently, three unrelated cationic groups (phosphonium, pyridinium, and thianthrenium), which can replace C-H bonds late stage, have been identified as precursors to various functional groups. This review will discuss the synthesis and application of these three salts with an emphasis on their use for LSF and application to medicinal chemistry.
引用
收藏
页码:10047 / 10060
页数:14
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