OXIDATION OF ALKENES BY A CHIRAL NON-PORPHYRINIC OXIDIZING CATALYST BASED ON THE BLEOMYCIN-FE(II) COMPLEX

被引:38
作者
SUGA, A
SUGIYAMA, T
OTSUKA, M
OHNO, M
SUGIURA, Y
MAEDA, K
机构
[1] UNIV TOKYO,FAC PHARMACEUT SCI,BUNKYO KU,TOKYO 113,JAPAN
[2] INST MICROBIAL CHEM,SHINAGAWA KU,TOKYO 141,JAPAN
[3] KYOTO UNIV,INST CHEM RES,UJI,KYOTO 611,JAPAN
关键词
D O I
10.1016/S0040-4020(01)86376-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A synthetic model for the metal binding site of bleomycin with 4-dimethylaminopyridine nucleus, namely PYML-8, shows dioxygen activation up to 125% of that of bleomycin. beta-Methylstyrene is oxidated with the Fe(III)-H2O2, Fe(III)-PhIO, or Fe(II)-O2 complex systems of PYML-8 to give a set of products including optically active epoxide. The product composition is dependent on iron, oxygen source, and reducing agent employed, suggesting varied active species generated from each complex system.
引用
收藏
页码:1191 / 1204
页数:14
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