首页> 外文期刊>Advanced synthesis & catalysis >Manganese Dioxide-Mediated Oxidative Coupling of 1,3-Dicarbonyl Compounds with α,β-Unsaturated Ketones: Direct Access to 3,4-DicarbonyI Substituted Furans
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Manganese Dioxide-Mediated Oxidative Coupling of 1,3-Dicarbonyl Compounds with α,β-Unsaturated Ketones: Direct Access to 3,4-DicarbonyI Substituted Furans

机译:1,3-二羰基化合物与α,β-不饱和酮的二氧化锰介导的氧化偶联:直接获得3,4-DicarbonyI取代的呋喃

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摘要

An efficient manganese dioxide-mediated and highly selective oxidative C—H/C—H functional-ization of 1,3-dicarbonyl compounds with α,β-unsa-turated ketones for the construction of tetrasubsti-tuted furans in one step has been demonstrated. This catalytic system converts two C—H bonds and G=O bonds to C=C and C—O bonds. This reaction provides a facile and regio-defined method for the synthesis of 3,4-dicarbonyl substituted furans.
机译:已经证明了有效的二氧化锰介导的高选择性氧化1,3-二羰基化合物与α,β-未取代的酮的C-H / C-H官能化反应,可一步构建四取代呋喃。 。该催化体系将两个CH键和G = O键转化为C = C键和CO键。该反应为3,4-二羰基取代的呋喃的合成提供了一种简便且按区域定义的方法。

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