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[1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes

机译:[1 + 1 + 1]环三聚反应合成环丙烷

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摘要

The synthesis of small rings by functionalization of C(sp(3))-H bonds remains a great challenge. We report for the first time a copper-catalyzed [1+1+1] cyclotrimerization of acetophenone derivatives under mild reaction conditions. The reaction has a broad scope for the stereoselective synthesis of cyclopropanes by trimerization of acetophenone. The developed transformation is based on an extraordinary copper-catalyzed cascade process that allows saturated carbocycles to be obtained for the first time by cyclotrimerization through functionalization of C(sp(3))-H bonds. The cascade of sixfold C(sp(3))-H bond functionalization allows the synthesis of cyclopropanes in a highly stereoselective approach.
机译:通过功能化的C(sp(3))-H键合成小环仍然是一个巨大的挑战。我们首次报告了在温和的反应条件下铜催化的苯乙酮衍生物的[1 + 1 + 1]环三聚。该反应对于通过苯乙酮的三聚来立体选择性地合成环丙烷具有广阔的范围。所开发的转化基于非凡的铜催化级联过程,该过程允许通过C(sp(3))-H键的官能团的环三聚作用首次获得饱和的碳环。级联的六倍C(sp(3))-H键功能化允许以高度立体选择性的方式合成环丙烷。

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