The molecular recognition of saccharides by synthetic hosts has become an appealing but elusive task in the last decades. Herein, we combine Dynamic Combinatorial Chemistry (DCC) for the rapid self-assembly and screening of virtual libraries of receptors, with the use of ITC and NMR to validate the hits and molecular modelling to understand the binding mechanisms. We discovered a minimalistic receptor, 1F (-benzyl-L-phenylalanine), with considerable affinity for fructose ( = 1762 M) and remarkable selectivity (>50-fold) over other common monosaccharides.
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