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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A novel MgI2 mediated unusual dimerization-spirocyclopropanation of bromo isomerised Morita-Baylis-Hillman adduct of isatin: a facile synthesis of 3-spirocyclopropane-2-oxindole derivatives
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A novel MgI2 mediated unusual dimerization-spirocyclopropanation of bromo isomerised Morita-Baylis-Hillman adduct of isatin: a facile synthesis of 3-spirocyclopropane-2-oxindole derivatives

机译:一种新型的MgI2介导的溴异构化的Isita的Morita-Baylis-Hillman加合物与寻常的二聚化-螺环丙烷化反应:3-螺环丙烷-2-氧吲哚衍生物的简便合成

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摘要

A novel magnesium iodide mediated unusual dimerization-spirocyclopropanation of bromo isomerised Morita-Baylis-Hillman adducts of isatin afforded highly functionalized 3-spirocyclopropane-2-oxindole derivatives as regioisomers in good combined yield. It has been observed that the regioselectivity is dependent on the nature of electron withdrawing group at the activated position. A plausible mechanism involving organomagnesium reagent has been proposed.
机译:新型的碘化镁介导的溴化异构化的森田-Baylis-Hillman加合物的异寻常的二聚化-螺环丙烷化反应,以区域异构体形式提供了高度功能化的3-螺环丙烷-2-氧吲哚衍生物,并具有良好的合成收率。已经观察到区域选择性取决于活化位置上的吸电子基团的性质。已经提出了涉及有机镁试剂的合理机理。

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