1210054-79-7Relevant articles and documents
Cross-couplings between benzylic and aryl halides on water : Synthesis of diarylmethanes
Duplais, Christophe,Krasovskiy, Arkady,Wattenberg, Alina,Lipshutz, Bruce H.
supporting information; experimental part, p. 562 - 564 (2010/05/01)
A remarkably simple entry to unsymmetrical diarylmethanes has been developed that relies on an in situ organozinc-mediated, palladium-catalyzed cross-coupling. Thus, by mixing a benzyl and aryl halide together in the presence of Zn metal and a Pd catalyst, diarylmethanes are formed at room temperature without assistance by a surfactant; hence, on water .