Issue 17, 2015

N-heterocyclic carbene–palladium(ii)-1-methylimidazole complex-catalyzed Suzuki–Miyaura coupling of benzyl sulfonates with arylboronic acids

Abstract

The first example of palladium-catalyzed Suzuki–Miyaura coupling between benzyl sulfonates and arylboronic acids was reported in this paper. In the presence of a well-defined, air-stable and easily available NHC–Pd(II)–Im complex, all reactions worked well to give the desired products in good to almost quantitative yields under the optimal conditions. Electron-rich, -neutral, -poor and sterically-hindered substituents on both substrates are tolerated in such transformation, providing a convenient, efficient and alternative method for the synthesis of diarylmethanes.

Graphical abstract: N-heterocyclic carbene–palladium(ii)-1-methylimidazole complex-catalyzed Suzuki–Miyaura coupling of benzyl sulfonates with arylboronic acids

Supplementary files

Article information

Article type
Paper
Submitted
27 Dec 2014
Accepted
19 Mar 2015
First published
19 Mar 2015

Org. Biomol. Chem., 2015,13, 4925-4930

N-heterocyclic carbene–palladium(II)-1-methylimidazole complex-catalyzed Suzuki–Miyaura coupling of benzyl sulfonates with arylboronic acids

X. Wang, B. Xu, W. Song, K. Sun and J. Lu, Org. Biomol. Chem., 2015, 13, 4925 DOI: 10.1039/C4OB02675F

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