Enantioselective epoxidation of conjugated Z-olefins with newly modified Mn(salen) complex

被引:12
|
作者
Egami, Hiromichi [1 ]
Irie, Ryo [1 ]
Sakai, Ken [1 ]
Katsuki, Tsutomu [1 ]
机构
[1] Kyushu Univ 33, Grad Sch, Fac Sci, Dept Chem,Higashi Ku, Fukuoka 8128581, Japan
关键词
D O I
10.1246/cl.2007.46
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral Mn(salen) complex 3 bearing a 1-ethyl-1-methylpropy1 group at C3, C3', C5, and C5' was found to induce higher asymmetry in the epoxidation of conjugated Z-olefins, especially less nucleophilic ones, in the presence of 4-phenylpyridine Noxide than complex 1 bearing a t-butyl group at the same carbons. The higher enantioselectivity was considered to be attributable to Me-in-plane conformation of the 1-ethyl-1-methylpropy1 group at C3 and C3'.
引用
收藏
页码:46 / 47
页数:2
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