The liquid phase synthesis of biaryls via Suzuki cross-coupling reacti
on on poly(ethylene glycol) supports (PEGs) is described. The reaction
is exemplified by parallel coupling of polymer bound aryl halides wit
h boronic acids. Four different PEGs were employed as soluble polymer
supports for parallel synthesis. The generated libraries include both
sterically hindered aryl halides (2b, 2d) and boronic acids. The react
ions were run in the homogeneous phase and the synthetic sequences per
formed in parallel fashion. Quantitative conversion in the Suzuki coup
lings was verified by H-1-NMR analysis (3a-r). The polymer bound produ
cts were isolated in good to excellent (52% to 98%) yields by either s
imple precipitation of the soluble support or column filtration.