二碘化钐在脱氧、还原和碳—碳键形成反应中的应用  

Some Application of Samarium Diiodide in Deoxygenation, Reduction and Carbon-Carbon Bond Formation Reaction

作　　者：张永敏[1] 林荣辉[1] 刘田春 

机构地区：[1]杭州大学化学系

出　　处：《化学学报》1990年第6期577-581,共5页Acta Chimica Sinica

基　　金：国家自然科学基金

摘　　要：本文研究了二碘化钐对一些有机化合物的脱氧反应,以及它在醇存在下对α-卤代酮、偶氮苯和苯醌的还原反应。首次报道了在二碘化钐作用下α-卤代酮与醛之间的碳—碳键形成反应,高产率地制备了各种α,β-不饱和酮;同时提出了涉及由α-卤代酮同时与Sm(Ⅱ)和Sm(Ⅲ)/Ⅰ^-物种作用形成烯醇钐盐中间体的可能机理。The deoxygenation and reduction of some organic substrates with samarium diiodide were investigated. The carbon—carbon bond formation between α-haloketone and aldehyde promoted by samarium diiodide was first reported. A possible mechanism involving samariun(Ⅲ) enolate intermediate formed in situ from α-haloketone with both Sm (Ⅱ) and Sm (Ⅲ)/Ⅰ^- species was proposed.

关 键 词：二碘化钐 有机化学反应 应用 

分 类 号：O614.337[理学—无机化学]