326-46-5Relevant articles and documents
Palladium-Catalyzed Carbonylative Esterification of Primary Alcohols with Aryl Chlorides through Dehydroxymethylative C-C Bond Cleavage
Park, Hyo-Soon,Kim, Dong-Su,Jun, Chul-Ho
, p. 397 - 401 (2015/04/27)
Aryl chlorides in the presence of Pd/C catalyst and NaF react with primary alcohols to form esters, arenes, and alkanes. In this reaction, aryl chlorides act as both oxidants and coupling partners, whereas alcohols serve as both carbonyl sources and alkoxy components of the ester products. (Formula Presented).
Nickel-mediated oxidative fluorination for PET with aqueous [ 18F] fluoride
Lee, Eunsung,Hooker, Jacob M.,Ritter, Tobias
, p. 17456 - 17458 (2013/01/15)
A one-step oxidative fluorination for carbon-fluorine bond formation from well-defined nickel complexes with oxidant and aqueous fluoride is presented, which enables a straightforward and practical 18F late-stage fluorination of complex small molecules with potential for PET imaging.