Murahashi Cross-Coupling at-78 °C: A One-Pot Procedure for Sequential C-C/C-C, C-C/C-N, and C-C/C-S Cross-Coupling of Bromo-Chloro-Arenes

被引:18
|
作者
Sinha, Narayan [1 ,3 ,4 ]
Heijnen, Dorus [1 ,2 ]
Feringa, Ben L. [2 ]
Organ, Michael G. [1 ,3 ,4 ]
机构
[1] York Univ, Dept Chem, 4700 Keele St, Toronto, ON M3J 1P3, Canada
[2] Univ Groningen, Stratingh Inst Chem, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
[3] Univ Ottawa, CCRI, Ottawa, ON K1N 6N5, Canada
[4] Univ Ottawa, Dept Chem & Biomol Sci, Ottawa, ON K1N 6N5, Canada
基金
欧洲研究理事会;
关键词
Murahashi coupling; organolithium; Pd catalysis; PEPPSI; sequential cross-coupling; ALKYL GRIGNARD-REAGENTS; PD-PEPPSI-IPENT; LOW-TEMPERATURE; ROOM-TEMPERATURE; EFFECTIVE CATALYST; NHC COMPLEXES; VINYL HALIDES; ARYL HALIDES; PD-PEPPSI-IPENT(CL); HETEROCYCLES;
D O I
10.1002/chem.201901678
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The coupling of organolithium reagents, including strongly hindered examples, at cryogenic temperatures (as low as -78 degrees C) has been achieved with high-reactivity Pd-NHC catalysts. A temperature-dependent chemoselectivity trigger has been developed for the selective coupling of aryl bromides in the presence of chlorides. Building on this, a one-pot, sequential coupling strategy is presented for the rapid construction of advanced building blocks. Importantly, one-shot addition of alkyllithium compounds to Pd cross-coupling reactions has been achieved, eliminating the need for slow addition by syringe pump.
引用
收藏
页码:9180 / 9184
页数:5
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