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首页> 外文期刊>Angewandte Chemie >Tertiary alpha-Silyl Alcohols by Diastereoselective Coupling of 1,3-Dienes and Acylsilanes Initiated by Enantioselective Copper-Catalyzed Borylation
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Tertiary alpha-Silyl Alcohols by Diastereoselective Coupling of 1,3-Dienes and Acylsilanes Initiated by Enantioselective Copper-Catalyzed Borylation

机译:由1,3-二烯和酰基硅烷的反映选择偶联的叔α-甲硅烷基醇和通过对映选择性的铜催化的促进促进型

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摘要

An efficient synthesis of functionalized tertiary alpha-silyl alcohols by an enantio- and diastereoselective copper-catalyzed three-component coupling of 1,3-dienes, bis(pinacolato)diboron, and acylsilanes is reported. The reaction proceeds well with different 1,3-dienes and a broad range of aryl- as well as alkenyl- but also alkyl-substituted acylsilanes. The target compounds are formed with high regio-, diastereo-, and enantioselectivity (up to 99 % ee and d.r. >20:1) and are highly versatile synthetic building blocks.
机译:通过对1,3-二烯(Pinacolato)二硼和酰基硅烷和酰基溶解的三分组分偶联的三分组分偶联的官能化叔α-甲硅烷基醇的有效合成。 该反应良好地进行良好的1,3-二烯和芳基 - 以及链烯基,但也是烷基取代的酰基硅烷。 目标化合物形成有高法官,非对映的和对映选择性(高达99%EE和D.R.> 20:1)形成,并且是高度通用的合成构建块。

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