69725-02-6Relevant academic research and scientific papers
Palladium-catalyzed double carbonylation using near stoichiometric carbon monoxide: Expedient access to substituted 13C2-labeled phenethylamines
Nielsen, Dennis U.,Neumann, Karoline,Taaning, Rolf H.,Lindhardt, Anders T.,Modvig, Amalie,Skrydstrup, Troels
experimental part, p. 6155 - 6165 (2012/09/21)
A novel and general approach for 13C2- and 2H-labeled phenethylamine derivatives has been developed, based on a highly convergent single-step assembly of the carbon skeleton. The efficient incorporation of two carbon-13 isotopes into phenethylamines was accomplished using a palladium-catalyzed double carbonylation of aryl iodides with near stoichiometric carbon monoxide.
Zinc chloride promoted formal oxidative coupling of aromatic aldehydes and isocyanides to α-ketoamides
Bouma, Marinus,Masson, Geraldine,Zhu, Jieping
supporting information; experimental part, p. 2748 - 2751 (2010/07/17)
Reaction of aromatic aldehydes and isocyanides in the presence of N-methylhydroxyamine, acetic acid, and zinc chloride affords the aryl α-ketoamides in moderate to good yields.
