CAS Key Laboratory of Receptor Research, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
J Org Chem. 2022 May 20;87(10):6807-6811. doi: 10.1021/acs.joc.2c00498. Epub 2022 May 4.
We report herein the synthesis of 1,3-enynes via palladium-catalyzed cross-coupling between enone derivatives and alkynylsilanes. The employment of an appropriate pyridine-oxazoline ligand is the key to the C-C cleavage and the high / stereoselectivity. This protocol features broad substrate scope and wide functional-group tolerance, affording the desired products in moderate-to-good yields. Late-stage diversification of natural product β-ionone further demonstrated the synthetic utility of this protocol.
我们在此报告了通过钯催化的烯酮衍生物和炔基硅烷之间的交叉偶联反应合成 1,3-烯炔的方法。合适的吡啶-噁唑啉配体的使用是 C-C 断裂和高立体选择性的关键。该方法具有广泛的底物范围和广泛的官能团容忍性,能够以中等至良好的收率得到所需产物。天然产物β-紫罗兰酮的后期多样化进一步证明了该方法的合成实用性。