Lundgren, Rylan J.; Peters, Brendan D.; Alsabeh, Pamela G.; Stradiotto, Mark published an article in 2010, the title of the article was A P,N-Ligand for Palladium-Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions.Electric Literature of 452-75-5 And the article contains the following content:
An air-stable P,N-ligand (I), that advances the scope and utility of palladium-catalyzed ammonia cross-coupling reactions, was developed. A variety of aryl chloride and aryl tosylate substrates can be coupled efficiently, most notably electron-rich species lacking ortho-substitution under a range of conditions. The unique preference for ammonia coupling when using Pd/I mixtures can be exploited in unprecedented chemoselective arylations, and for the first time, the room temperature palladium-catalyzed cross-coupling of ammonia has been achieved. The experimental process involved the reaction of 4-Chloro-2-fluorotoluene(cas: 452-75-5).Electric Literature of 452-75-5
The Article related to arylamine preparation, palladium catalyst ammonia cross coupling reaction aryl chloride tosylate, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Amines, Amine Oxides, Imines, and Quaternary Ammonium Compounds and other aspects.Electric Literature of 452-75-5
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics