Li Feng, Ma Juan, Wang Nana
Key Laboratory for Soft Chemistry and Functional Materials, Ministry of Education, Nanjing University of Science and Technology , Nanjing 210094, People's Republic of China.
J Org Chem. 2014 Nov 7;79(21):10447-55. doi: 10.1021/jo502051d. Epub 2014 Oct 23.
A CpIr complex bearing a functional bipyridonate ligand was found to be a highly effective and versatile catalyst for the α-alkylation of ketones with primary alcohols under extremely environmentally benign and mild conditions (0.1 equiv of Cs2CO3 per substrate, reflux in tert-amyl alcohol under an air atmosphere for 6 h). Furthermore, this complex also exhibited a high level of catalytic activity for the α-methylation of ketones with methanol. The mechanistic investigation revealed that the carbonyl group on the ligand is of critical importance for catalytic hydrogen transfer. Notably, the results of this study revealed the unique potential of CpIr complexes bearing a functional bipyridonate ligand for the development of C-C bond-forming reactions with the activation of primary alcohols as electrophiles.
发现一种带有功能性联吡啶酮配体的CpIr配合物是一种高效且通用的催化剂,可在极其环境友好和温和的条件下(每底物0.1当量的Cs2CO3,在空气气氛下于叔戊醇中回流6小时)实现酮与伯醇的α-烷基化反应。此外,该配合物对酮与甲醇的α-甲基化反应也表现出高水平的催化活性。机理研究表明,配体上的羰基对于催化氢转移至关重要。值得注意的是,本研究结果揭示了带有功能性联吡啶酮配体的CpIr配合物在开发以伯醇作为亲电试剂进行C-C键形成反应方面的独特潜力。