化学
硼酸
催化作用
背景(考古学)
联轴节(管道)
药物化学
有机化学
组合化学
高分子化学
冶金
生物
古生物学
材料科学
作者
Mark Stradiotto,Ryan S. Sawatzky
出处
期刊:Synlett
[Georg Thieme Verlag KG]
日期:2018-01-02
卷期号:29 (06): 799-804
被引量:22
标识
DOI:10.1055/s-0036-1591523
摘要
The successful application of (DPEPhos)Ni(mesityl)Br (C1) as a pre-catalyst in the Suzuki–Miyaura cross-coupling of heteroaryl chlorides or bromides and heteroaryl boronic acids is reported. The use of C1 in this context allows for such reactions to be conducted under mild conditions (2 mol% Ni, 25 °C), including cross-couplings leading to unsymmetrical biheteroaryls. Successful transformations of this type involving problematic pyridinyl boronic acid substrates (10 mol% Ni, 60 °C) are also described.
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