自行车
化学
烯丙基重排
过氧化氢
催化作用
区域选择性
环己烯
反应中间体
反应性(心理学)
药物化学
光化学
有机化学
金属
医学
病理
替代医学
作者
Xenia Engelmann,Deesha D. Malik,Teresa Corona,Katrin Warm,Erik R. Farquhar,Marcel Swart,Wonwoo Nam,Kallol Ray
标识
DOI:10.1002/anie.201812758
摘要
Abstract The generation of a nonheme oxoiron(IV) intermediate, [(cyclam)Fe IV (O)(CH 3 CN)] 2+ ( 2 ; cyclam=1,4,8,11‐tetraazacyclotetradecane), is reported in the reactions of [(cyclam)Fe II ] 2+ with aqueous hydrogen peroxide (H 2 O 2 ) or a soluble iodosylbenzene ( s PhIO) as a rare example of an oxoiron(IV) species that shows a preference for epoxidation over allylic oxidation in the oxidation of cyclohexene. Complex 2 is kinetically and catalytically competent to perform the epoxidation of olefins with high stereo‐ and regioselectivity. More importantly, 2 is likely to be the reactive intermediate involved in the catalytic epoxidation of olefins by [(cyclam)Fe II ] 2+ and H 2 O 2 . In spite of the predominance of the oxoiron(IV) cores in biology, the present study is a rare example of high‐yield isolation and spectroscopic characterization of a catalytically relevant oxoiron(IV) intermediate in chemical oxidation reactions.
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