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Updated: Dec 3, 2025

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
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Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

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Recent Advances in Palladium-Catalyzed Isocyanide Insertions.

Jurriën W Collet1,2, Thomas R Roose1, Bram Weijers1

  • 1Department of Chemistry and Pharmaceutical Sciences and Amsterdam Institute for Molecules, Medicines & Systems (AIMMS), Vrije Universiteit Amsterdam, De Boelelaan 1108, 1081 HZ Amsterdam, The Netherlands.

Molecules (Basel, Switzerland)
|October 29, 2020
PubMed
Summary

Isocyanides are versatile C1 building blocks in organic synthesis. Recent palladium-catalyzed reactions significantly expand their use in imidoylative cross-couplings, incorporating nitrogenous fragments.

Keywords:
catalysisheterocyclesinsertion reactionsisocyanidespalladium

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