What role does the acetoxy group at the 3-position of cephalosporins have in enhancing antibacterial activity?
It acts as a good leaving group when the b-lactam ring is opened
It takes part in a transesterification reaction with the carboxylic acid group at position 4
It increases the reactivity of the b-lactam ring by neighbouring group participation
It acts as a steric shield and masks enzymatic attack at the b-lactam ring
What role does the acetoxy group at the 3-position of cephalosporins have in enhancing antibacterial activity?...