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Molecular Self‐Assembly of Cyclic Dipeptide Derivatives and Their Applications
Cyclic dipeptides (CDPs) are heterocyclic 2,5‐diketopiperazines with exceptional structural rigidity, enzymatic stability, and biological activity, exhibiting a substantial tendency to take part in intermolecular interactions. Strong intermolecular interactions driven by unique hydrogen bonding patt...
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Published in: | ChemPlusChem (Weinheim, Germany) Germany), 2017-01, Vol.82 (1), p.88-106 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Cyclic dipeptides (CDPs) are heterocyclic 2,5‐diketopiperazines with exceptional structural rigidity, enzymatic stability, and biological activity, exhibiting a substantial tendency to take part in intermolecular interactions. Strong intermolecular interactions driven by unique hydrogen bonding patterns render CDPs with a high propensity to undergo molecular self‐assembly. In this Review, the aim is to provide a comprehensive summary of design strategies used to engineer the molecular self‐assembly of CDPs into functional nano‐ and micro‐architectures and molecular gels with potential applications in biomedical and materials engineering fields.
Robust synthons: Cyclic dipeptides (CDPs) are 2,5‐diketopiperazines with exceptional structural rigidity, enzymatic stability and biological activity. CDPs are robust platforms for molecular self‐assembly owing to their propensity to engage in intermolecular hydrogen bonding and other noncovalent interactions. Recent advances in engineering functional architectures of CDPs and their prospective applications are discussed. |
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ISSN: | 2192-6506 2192-6506 |
DOI: | 10.1002/cplu.201600450 |