Volla Chandra M R, Bäckvall Jan-E
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University , SE-10691 Stockholm, Sweden.
ACS Catal. 2016 Oct 7;6(10):6398-6402. doi: 10.1021/acscatal.6b02070. Epub 2016 Aug 23.
Herein we report a highly efficient and site-selective palladium-catalyzed oxidative carbocyclization-arylation reaction of bisallenes and arylboronic acids under operationally simple conditions for the selective synthesis of cyclohexadiene derivatives. The palladium source and the solvent proved to be crucial for the selectivity and the reactivity displayed. Interestingly, in the absence of the nucleophile, an oxidative carbocyclization-β-elimination pathway predominates. The reaction conditions are compatible with a wide range of functional groups, and the reaction exhibits broad substrate scope. Furthermore, key information regarding the mechanism was obtained using control experiments and kinetic studies.
在此,我们报道了一种高效且位点选择性的钯催化双烯丙基与芳基硼酸的氧化碳环化-芳基化反应,该反应在操作简单的条件下用于选择性合成环己二烯衍生物。事实证明,钯源和溶剂对于所表现出的选择性和反应活性至关重要。有趣的是,在没有亲核试剂的情况下,氧化碳环化-β-消除途径占主导。该反应条件与多种官能团兼容,并且反应具有广泛的底物范围。此外,通过对照实验和动力学研究获得了有关反应机理的关键信息。