Chung, Mee-KyungSeverin, KayLee, Stephen J.Waters, Marcey L.Gagné, Michel R.2011-03-102011-03-10201110.1039/C0SC00548Ghttps://infoscience.epfl.ch/handle/20.500.14299/65247WOS:000288387600024Mixtures of dipeptide monomers create stereochemically and constitutionally complex dynamic libraries of potential receptors. When (−)-cytidine was utilized as guest an 84-membered cyclic host was amplified (70–175 fold) from a nearly undetectable initial concentration. Only the specified diastereomeric combination of the two chiral building blocks yielded a dynamic library from which the macrocyclic receptor could be amplified.Dynamic Combinatorial LibrariesDiastereoselective AmplificationSystems ChemistryBuilding-BlocksGuest BindingReceptorsDiscoverytext::journal::journal article::research article