Lee Hyojae, Lee Yeosan, Cho Seung Hwan
Department of Chemistry , Pohang University of Science and Technology (POSTECH) , Pohang , 37673 , Republic of Korea.
Org Lett. 2019 Aug 2;21(15):5912-5916. doi: 10.1021/acs.orglett.9b02050. Epub 2019 Jul 22.
We describe a palladium-catalyzed chemoselective Negishi cross-coupling of a bis[(pinacolato)boryl]methylzinc halide with aryl (pseudo)halides. This reaction affords an array of benzylic 1,1-diboronate esters, which can serve as useful synthetic handles for further transformations. The developed coupling reaction is compatible with various functional groups and can be easily scaled up. The coupling of bis[(pinacolato)boryl]methylzinc halides with pharmaceuticals and the subsequent late-stage manipulations demonstrate the power of the developed protocol.
我们描述了一种钯催化的双[(频哪醇硼酸酯)硼基]甲基卤化锌与芳基(拟)卤化物的化学选择性根岸交叉偶联反应。该反应提供了一系列苄基1,1-二硼酸酯,它们可作为进一步转化的有用合成中间体。所开发的偶联反应与各种官能团兼容,并且易于放大规模。双[(频哪醇硼酸酯)硼基]甲基卤化锌与药物的偶联以及随后的后期操作证明了所开发方法的实用性。