The iodination of heterocyclic compounds has significant interest in synthetic organic chemistry, as it provides versatile and efficient pathways for the synthesis of a wide range of biologically active molecules. This review aims to highlight recent advances in the iodination of heterocyclic compounds using elemental iodine or iodide‐based reagents, covering developments reported over the past 17 years.
Ajvazi et al. (Fri,) studied this question.