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Development of Ferrier(II) Carbocyclization Catalyzed by Pd(II) and Its Application to the Synthesis of Bioactive Substances

机译:Pd(II)催化的二价碳酰化载体的开发及其在生物活性物质合成中的应用

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摘要

Highly functionalized cyclohexanes are useful intermediates for the synthesis of natural products and their derivatives having 6-membered ring systems. Among the preparation of chiral substituted cyclohexanes. Hg(II) salts mediated conversion of aldohexoses into cyclohexanones [Ferrier (II) carbocyclization] has become one of the most efficient and intriguing process. This article summarizes our recent works concerning the development of the catalytic Ferrier(II) carbocyclization mediated by Pd(II) salts and the application of this reaction to the total syntheses: i) #beta#-glucosidase inhibitor, cyclophellitol, ii) all diastereoisomers of inositol and D-myo-inositol phosphates. It should be emphasized that PdCl_2-mediated transformation enabled us to prepare such expensive inositol derivatives efficiently.
机译:高度官能化的环己烷是合成天然产物及其具有六元环系统的衍生物的有用中间体。其中有制备手性取代的环己烷。 Hg(II)盐介导的醛糖己糖向环己酮的转化[Ferrier(II)碳环化]已成为最有效,最有趣的过程之一。本文总结了我们最近有关由Pd(II)盐介导的催化Ferrier(II)碳环化的发展以及该反应在总合成中的应用的最新工作:i)#β#-葡萄糖苷酶抑制剂,环糖醇,ii)所有非对映异构体肌醇和D-肌醇磷酸酯应该强调的是,PdCl_2介导的转化使我们能够有效地制备出如此昂贵的肌醇衍生物。

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