arom68
Hiya synthetic folks!
I am trying to carry a Suzuki rxn out on an aryl halide and a tbutyldiphenylsilyl- protected phenyl boronic acid but I have read that the protecting group would not survive alkalinity of the reaction. Any suggestions to get around this?
I am trying to carry a Suzuki rxn out on an aryl halide and a tbutyldiphenylsilyl- protected phenyl boronic acid but I have read that the protecting group would not survive alkalinity of the reaction. Any suggestions to get around this?