Pd-Catalysed carbonylative Suzuki–Miyaura cross-couplings using Fe(CO) 5 under mild conditions: generation of a highly active, recyclable and scalable ‘Pd–Fe’ nanocatalyst

Zhu, Z., Wang, Z., Jian, Y. , Sun, H., Zhang, G., Lynam, J.M., McElroy, Con, Burden, T.J., Inight, R.L., Fairlamb, I.J.S., Zhang, W. and Gao, Z. (2021) Pd-Catalysed carbonylative Suzuki–Miyaura cross-couplings using Fe(CO) 5 under mild conditions: generation of a highly active, recyclable and scalable ‘Pd–Fe’ nanocatalyst. Green Chemistry, 23 (2). pp. 920-926. ISSN 1463-9262

Full content URL: https://doi.org/10.1039/d0gc03036h

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Item Type:Article
Item Status:Live Archive

Abstract

The dual function and role of iron(0) pentacarbonyl Fe(CO)5 has been identified in gaseous CO-free carbonylative Suzuki-Miyaura cross-couplings, in which Fe(CO)5supplied COin situ, leading to the propagation of catalytically active Pd-Fe nanoparticles. Compared with typical carbonylative reaction conditions, CO gas (at high pressures), specialised exogenous ligands and inert reaction conditions were avoided. Our developed reaction conditions are mild, do not require specialised CO high pressure equipment, and exhibit wide functional group tolerance, giving a library of biaryl ketones in good yields.

Additional Information:cited By 6
Keywords:palladium, Suzuki-Miyaura coupling
Subjects:F Physical Sciences > F100 Chemistry
Divisions:College of Science > School of Chemistry
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ID Code:54737
Deposited On:30 May 2023 13:53

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