Total synthesis of non-natural compounds for molecular recognition. the double challenge

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Abstract

Molecular recognition of biomolecules by synthetic receptors requires modular assembly of various components to complement the molecular characteristics (sizes, topologies, and functional groups) of the substrate. A number of receptors for biorelevant molecules containing oxoanions have been assembled from a bicyclic chiral guanidine subunit. Several receptors accelerate or catalyze reactions proceeding through anionic transition states. Among the structures recently prepared, a receptor incorporating a calix[6]arene subunit has been developed, showing high affinity for phosphocholine derivatives. Chains of tetraguanidinium sulfates form double helices in solution. These substances strongly induce formation of α-helical conformations in Asp rich peptides.

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De Mendoza, J., Alcázar, V., Botana, E., Galán, A., Lu, G., Magrans, J. O., … Segura, M. (1997). Total synthesis of non-natural compounds for molecular recognition. the double challenge. Pure and Applied Chemistry, 69(3), 577–582. https://doi.org/10.1351/pac199769030577

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