The reactivity of an unusual enamide functional group in the nucleoside antibiotic mureidomycin A (MRD A) has been investigated by synthesis of enamide-containing analogues. Enamides based on 2-methoxyethylamine and tetrahydrofurfurylamine were found to be unstable and reactive, whereas a uridine-based analogue showed high stability and low reactivity. Samples of mureidomycin A and the uridine-based analogue were ...
[Charville, Hayley; Jackson, David A.; Hodges, George; Whiting, Andrew; Wilson, Mark R. European Journal of Organic Chemistry, 2011 , # 30 p. 5981 - 5990]