Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Kyoto 615-8510, Japan.
J Am Chem Soc. 2012 Feb 29;134(8):3699-702. doi: 10.1021/ja3002953. Epub 2012 Feb 17.
Pyridine undergoes addition of pinacolborane at 50 °C in the presence of a rhodium catalyst, giving N-boryl-1,2-dihydropyridine in a high yield. The selective 1,2-hydroboration also takes place in the reactions of substituted pyridines. In the reaction of 3-substituted pyridines, 3-substituted N-boryl-1,2-dihydropyridines are formed regioselectively.
吡啶在 50°C 下在铑催化剂的存在下与频哪醇硼烷加成,以高产率得到 N-硼代-1,2-二氢吡啶。取代吡啶的反应也发生选择性 1,2-硼氢化反应。在 3-取代吡啶的反应中,3-取代的 N-硼代-1,2-二氢吡啶以区域选择性方式形成。