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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >STILLE CROSS-COUPLING REACTIONS OF ARYL MESYLATES AND TOSYLATES USING A BIARYLPHOSPHINE BASED CATALYST SYSTEM
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STILLE CROSS-COUPLING REACTIONS OF ARYL MESYLATES AND TOSYLATES USING A BIARYLPHOSPHINE BASED CATALYST SYSTEM

机译:芳基甲磺酸盐和甲苯磺酸盐在双芳烃基催化剂体系中的静态交叉偶联反应

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摘要

A catalyst system for the Stille cross-coupling reactions of aryl mesylates and tosylates is reported. Using the combination of Pd(OAc)2, XPhos, and CsF in t-BuOH an array of aryl and heteroaryl sulfonates were successfully employed in these reactions. Morever, heteroarylstannanes, such as furyl, thienyl, and N-methylpyrrolyl, which are often prone to decomposition, were efficiently coupled under these conditions. Ortho-substitution on the stannane coupling partner was well tolerated; however, the presence of ortho substituents on the aryl sulfonates greatly reduced the efficiency of these reactions.
机译:报道了用于甲磺酸甲磺酸酯和甲苯磺酸酯的Stille交叉偶联反应的催化剂体系。使用Pd(OAc)2,XPhos和CsF在t-BuOH中的组合,在这些反应中成功使用了芳基和杂芳基磺酸盐的阵列。此外,经常易于分解的杂芳基锡烷,例如呋喃基,噻吩基和N-甲基吡咯基,在这些条件下被有效地偶联。锡烷偶联伴侣的邻位取代耐受性良好。然而,芳基磺酸盐上邻位取代基的存在大大降低了这些反应的效率。

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