An Investigation into Causes and Effects of High Cyanide Levels in the Palladium-Catalyzed Cyanation Reaction
Organic Letters2004Vol. 6(21), pp. 3723–3725
Citations Over TimeTop 10% of 2004 papers
Karen Marcantonio, Lisa Frey, Yong Liu, Yadan Chen, Jeff Strine, Brian D. Phenix, Debra J. Wallace, Cheng‐yi Chen
Abstract
[reaction: see text] The palladium-catalyzed cyanation reaction is known to be sensitive to dissolved cyanide. Investigation into some causes of high levels of dissolved cyanide is presented here, along with a robust solution to this problem.
Related Papers
- → Direct cyanation, hydrocyanation, dicyanation and cyanofunctionalization of alkynes(2020)37 cited
- → Rhodium(iii)-catalyzed cyanation of vinylic C–H bonds: N-cyano-N-phenyl-p-toluenesulfonamide as a cyanation reagent(2015)61 cited
- → Ni-Catalyzed C–H Cyanation of (Hetero)arenes with 2-Cyanoisothiazolidine 1,1-Dioxide as a Cyanation Reagent(2021)14 cited
- → Efficient Synthesis of Aromatic Nitriles via Cyanation of Aryl Bromides and K<sub>4</sub>[Fe(CN)<sub>6</sub>] Catalyzed by a Palladium(II) Complex(2013)8 cited
- → Palladium-Catalyzed Direct Cyanation of Indoles with K4[Fe(CN)6](2010)