Asymmetric reactions involving aryne intermediates

被引:13
|
作者
Kamikawa, Ken [1 ]
机构
[1] Osaka Metropolitan Univ, Grad Sch Sci, Dept Chem, Sakai, Osaka, Japan
关键词
AMINO-ACID DERIVATIVES; DIELS-ALDER REACTIONS; ENE REACTION; ALPHA-ARYLATION; ENANTIOSELECTIVE CONSTRUCTION; ATROPOSELECTIVE SYNTHESIS; COUPLING REACTIONS; METAL-COMPLEXES; PHENYL-LITHIUM; MEMORY;
D O I
10.1038/s41570-023-00485-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although arynes are usually considered fleeting intermediates, they are highly valuable synthons because they enable the introduction of aromatic rings and the simultaneous formation of new bonds at two sites. Although catalytic reactions using transition metals are excellent method for constructing complex polycyclic aromatic molecules in a single step, the use of asymmetric catalysis for the capture of arynes remains a crucial goal for the progress of aryne chemistry. Catalytic asymmetric reactions of arenes are challenging, requiring sufficient interactions between the neutral and highly reactive short-lived aryne intermediates in a stereo-controlled fashion. In addition, spontaneous decomposition, as well as side reactions, has hindered their development and, until recently, highly enantioselective reactions using arynes had remained elusive. This Review highlights asymmetric reactions using arynes, featuring diastereoselective, enantioselective and catalytic enantioselective reactions. [GRAPHICS] .
引用
收藏
页码:496 / 510
页数:15
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