Merging kinetic resolution with C-H activation: an efficient approach for enantioselective synthesis

被引:16
|
作者
Sumit [1 ,2 ]
Chandra, Devesh [1 ,2 ]
Sharma, Upendra [1 ,2 ]
机构
[1] IHBT, CSIR, Chem Technol Div, Palampur 176061, HP, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
关键词
45;
D O I
10.1039/d1ob00232e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In the last two decades tremendous progress has been made in transition-metal (TM)-catalyzed C-H bond functionalization, paving the way to design complex molecules. Despite significant advances, enantioselective C-H activation is still in the age of infancy. For the enantioselective synthesis, several TM catalyst based approaches are well known, including kinetic resolution (KR) and its advanced versions [dynamic kinetic resolution (DKR) and parallel kinetic resolution (PKR)]. These strategies have recently been successfully applied synergetically with the TM catalyzed C-H activation to achieve enantioselective synthesis in a more economical and sustainable way. This review will summarize the recent advancements made towards merging KR with TM-catalysed C-H activation for enantioselective synthesis.
引用
收藏
页码:4014 / 4026
页数:13
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