Molecules (Oct 2020)

Recent Advances in Palladium-Catalyzed Isocyanide Insertions

  • Jurriën W. Collet,
  • Thomas R. Roose,
  • Bram Weijers,
  • Bert U. W. Maes,
  • Eelco Ruijter,
  • Romano V. A. Orru

DOI
https://doi.org/10.3390/molecules25214906
Journal volume & issue
Vol. 25, no. 21
p. 4906

Abstract

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Isocyanides have long been known as versatile chemical reagents in organic synthesis. Their ambivalent nature also allows them to function as a CO-substitute in palladium-catalyzed cross couplings. Over the past decades, isocyanides have emerged as practical and versatile C1 building blocks, whose inherent N-substitution allows for the rapid incorporation of nitrogeneous fragments in a wide variety of products. Recent developments in palladium catalyzed isocyanide insertion reactions have significantly expanded the scope and applicability of these imidoylative cross-couplings. This review highlights the advances made in this field over the past eight years.

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