Ontology highlight
ABSTRACT:
SUBMITTER: Duplais C
PROVIDER: S-EPMC3152455 | biostudies-literature | 2010 Jan
REPOSITORIES: biostudies-literature
Duplais Christophe C Krasovskiy Arkady A Wattenberg Alina A Lipshutz Bruce H BH
Chemical communications (Cambridge, England) 20091209 4
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". ...[more]