ɑ-Squaric Acid Ester Amido-ω-Tritylmercaptopropanamido PEG

PEGs with an active ester functional group at one end allow for selective and covalent attachment to other molecules with complementary functional groups, such as primary amines on proteins, peptides, or other molecules. To a lesser extent they are reactive towards thiols or hydroxyls (to form thioesters or esters). Squaric Acid Ester Amido PEGs are a novel class of reactive and chemoselective PEG crosslinking reagents. The squaric acid PEGs are chemoselective towards the amino groups of Lysin in protein PEGylation whereas the guanidine function of Arginine, the hydroxyl group of Serine and the imidazole function of Histidine are not affected. Compared to other active esters, these PEGs are remarkably stable in aqueous media and not easily hydrolyzed. PEG tritylthio derivatives feature a protected thiol at on chain end. Trityl groups are easily removed with acid. Pure TFA or TFA/DCM mixtures cleave trityl from thiols quantitatively.