“…The most commonly employed method for the functionalization of SubPcs is to replace the original axial Cl or Br atom by alcohols to yield the corresponding boronic esters. It is generally acknowledged that phenols [see refs , , , , − , − , − , , , , , , − , , , , , , , , , and − ] and carboxylic acids , react more efficiently than water or alkyl alcohols, ,,,,,,,,, despite their lower nucleophilicity, which suggests the assistance of relatively acidic protons in the weakening of the B–X bond.…”