New Directions in Transition Metal Catalyzed Carbonylation Chemistry

Authors

  • Dennis U. Nielsen Carbon Dioxide Activation Center (CADIAC) Interdisciplinary Nanoscience Center (iNANO) Department of Chemistry, Aarhus University Gustav Wieds Vej 14, 8000 Aarhus C, Denmark
  • Karoline T. Neumann Carbon Dioxide Activation Center (CADIAC) Interdisciplinary Nanoscience Center (iNANO) Department of Chemistry, Aarhus University Gustav Wieds Vej 14, 8000 Aarhus C, Denmark
  • Troels Skrydstrup Carbon Dioxide Activation Center (CADIAC) Interdisciplinary Nanoscience Center (iNANO) Department of Chemistry, Aarhus University Gustav Wieds Vej 14, 8000 Aarhus C, Denmark;, Email: ts@chem.au.dk

DOI:

https://doi.org/10.2533/chimia.2018.606

Keywords:

Carbonylation, Catalysis, Fluorination, Isotope labeling, Nickel, Palladium

Abstract

Carbon monoxide (CO) represents an important C1-building block for the construction of some of the most fundamental chemical functionalities carrying a carbon–oxygen double bond. Transition metal catalysis plays a key role in promoting such transformations. We have earlier shown that the combination of palladium catalysis with CO releasing molecules and the two-chamber reactor, COware, provides a convenient and safe means for performing traditional Pd-catalyzed carbonylative couplings, as well as being a platform for the discovery of new carbonylation reactions. Furthermore, the method can be adapted to 13C- and 14C-isotope labeling, as well as providing for a suitable setting for developing efficient carbonylation reactions with 11CO. Herein, we provide a short overview of our latest findings in this area with emphasis on carbonylative couplings with fluorinated building blocks, but also discuss our efforts to develop viable Ni-catalyzed carbonylations with aliphatic substrates, which can be performed efficiently under low CO partial pressures.

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Published

2018-09-01

How to Cite

[1]
D. U. Nielsen, K. T. Neumann, T. Skrydstrup, Chimia 2018, 72, 606, DOI: 10.2533/chimia.2018.606.