Zinc-Catalyzed Borylation of Primary, Secondary and Tertiary Alkyl Halides with Alkoxy Diboron Reagents at Room Temperature

被引:188
作者
Bose, Shubhankar Kumar [1 ]
Fucke, Katharina [1 ]
Liu, Lei [2 ]
Steel, Patrick G. [3 ]
Marder, Todd B. [1 ]
机构
[1] Univ Wurzburg, Inst Anorgan Chem, D-97074 Wurzburg, Germany
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] Univ Durham, Dept Chem, Durham DH1 3LE, England
关键词
boronate esters; cross-coupling; homogeneous catalysis; N-heterocyclic carbenes; Suzuki-Miyaura; ALPHA; BETA-UNSATURATED CARBONYL-COMPOUNDS; CROSS-COUPLING REACTIONS; RING-EXPANSION; DIORGANOZINC REAGENTS; ALKYLBORONIC ESTERS; ARYL HALIDES; COMPLEXES; DFT; HYDROBORATIONS; 1,4-DIBORATION;
D O I
10.1002/anie.201308855
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new catalytic system based on a Zn-II NHC precursor has been developed for the cross-coupling reaction of alkyl halides with diboron reagents, which represents a novel use of a GroupXII catalyst for CX borylation. This approach gives borylations of unactivated primary, secondary, and tertiary alkyl halides at room temperature to furnish alkyl boronates, with good functional-group compatibility, under mild conditions. Preliminary mechanistic investigations demonstrated that this borylation reaction seems to involve one-electron processes.
引用
收藏
页码:1799 / 1803
页数:5
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