Affiliation:
1. Department of Organic Chemistry University of Belgrade – Faculty of Pharmacy Belgarde Serbia
2. Department of Pharmaceutical Chemistry University of Belgrade – Faculty of Pharmacy Belgarde Serbia
Abstract
AbstractHydantoin derivatives are versatile structural motifs found in natural products and various compounds with different biological or other properties. Due to their importance in both organic and medicinal chemistry, a number of synthetic procedures have been developed. In this article, a novel methodology utilizing N‐Boc protected amino acid amides for their preparation has been described. The cyclisation process was accomplished using solid supported PPh3 and CBr4 as reagents affording substituted hydantoins in moderate to good yields (40%–77%).