Development of reaction using imines as a radical acceptor and its stereocontrol

被引:20
作者
Miyabe, H [1 ]
Naito, T [1 ]
机构
[1] Kobe Pharmaceut Univ, Kobe, Hyogo 6588558, Japan
关键词
radical; imine; oxime ether; amino acid; triethylborane; diethylzinc; one-pot; multi-component; asymmetric synthesis; solid-phase;
D O I
10.5059/yukigoseikyokaishi.59.33
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This review summarizes the recent progress in the field of radical reaction of imine derivatives, and focuses on the new carbon-carbon bond constructing-methods especially based on intermolecular carbon radical addition to imine derivatives. Among the wide range of radical accepters containing a carbon-nitrogen double bond, it was revealed that the oxime ethers were excellent radical accepters, and a lot of studies have been explored by using oxime ethers. Reactivity of imine derivatives and possible reaction pathways have also been presented. The reaction was extended to one-pot and/or multi-component reactions. Moreover, a high degree of stereocontrol in reaction of acyclic and cyclic imine derivatives was achieved by using triethylborane and diethylzinc.
引用
收藏
页码:33 / 39
页数:7
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