On April 13, 2011, Hesp, Kevin D.; Lundgren, Rylan J.; Stradiotto, Mark published an article.Recommanded Product: 4-Chloro-2-fluorotoluene The title of the article was Palladium-Catalyzed Mono-α-arylation of Acetone with Aryl Halides and Tosylates. And the article contained the following:
The first example of selective Pd-catalyzed mono-α-arylation of acetone employing aryl chlorides, bromides, iodides, and tosylates is reported. The use of appropriately designed P,N-ligands proved to be the key to controlling the reactivity and selectivity. The reaction affords good yields with substrates containing a range of functional groups at modest Pd loadings using Cs2CO3 as the base and employing acetone as both a reagent and the solvent. The experimental process involved the reaction of 4-Chloro-2-fluorotoluene(cas: 452-75-5).Recommanded Product: 4-Chloro-2-fluorotoluene
The Article related to aryl methyl ketone preparation, arylhalide acetone monoarylation palladium catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Recommanded Product: 4-Chloro-2-fluorotoluene
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics