硼酸化
芳基
卤化物
催化作用
化学
组合化学
电泳剂
有机化学
烷基
作者
Charissa Munteanu,Taylor E. Spiller,Jun Qiu,Albert J. DelMonte,Steven R. Wisniewski,Eric M. Simmons,Doug E. Frantz
标识
DOI:10.1021/acs.joc.0c00929
摘要
). For the Pd-based catalyst systems, we have identified general reaction conditions that allow for the sequestration of halide ions through simple precipitation that results in catalyst loadings as low as 0.01 mol % (100 ppm) and reaction temperatures as low as room temperature. We also describe a complementary Ni-based catalyst system that employs simple unligated Ni(II) salts as an inexpensive alternative to the Pd-based systems for the borylation of aryl (pseudo)halides. Extrapolation of all three systems to a one-pot tandem borylation/Suzuki-Miyaura cross-coupling is also demonstrated on advanced intermediates and drug substances.
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