“…47 This was also achieved by synthesizing a polymerizable template, a phenolic R-amphetamine sulfonamide derivative, that was combined with phenol and formaldehyde, the sulfonamide linkage being further hydrolyzed to provide cavities for the trapping of R-amphetamine. 40 Boronic acid was also used for its ability to form a reversible covalent complex with cis-diol compounds such as luteolin, 48,49 vitamin B12, 50 sialic acid, 51 or for the specific trapping of glycans of glycoproteins as discussed in more detail below. Many works reported the screening of different synthesis conditions by preparing MIPs using different types of monomers, cross-linkers, template/monomer or monomer/cross-linker ratios, natures of the porogen, 28,30,39,43,[52][53][54][55][56][57][58][59][60][61][62][63][64][65] and even the pH when boronic acid is involved.…”