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From the same journal

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

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Publication details

JournalGreen Chemistry
DateAccepted/In press - 23 Nov 2020
DatePublished (current) - 21 Jan 2021
Issue number2
Volume23
Number of pages7
Pages (from-to)920-926
Original languageEnglish

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.

Bibliographical note

Funding Information:
This work was supported by the grant from the National Natural Science Foundation of China (21371112 and 21446014), the 111 Project (B14041), the Fundamental Funds Research for the Central Universities (No. GK201501005, GK201503029, and 2016CSY002), the grant from the Fundamental Doctoral Fund of Ministry of Education of China (20120202120005), and the Program for Changjiang Scholars and Innovative Research Team in University (IRT_14R33). I. J. S. F. is grateful to the Royal Society for University Research Fellowship (2004-12). We thank Syngenta and the University of York for the iCASE funding and studentship to T. J. B. We also acknowledge the Leverhulme Trust for funding, enabling us to initiate this research (W. Z., I. J. S. F., and J. M. L.).

Publisher Copyright:
© The Royal Society of Chemistry 2021.

Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.

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