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- W2365004724 endingPage "6048" @default.
- W2365004724 startingPage "6037" @default.
- W2365004724 abstract "The importance of chiral compounds has been widely recognized. Enantioselectively controlled release of the desired enantiomer from a racemate while retarding the other isomer provides a novel route toward practical applications of biologically chiral molecules. Such processes may maximize the efficacy while minimizing the dosage and frequency of chiral compounds. So far, exciting achievements have been made in enantioselective release (ESR), which can be classified into two main groups according to the essential strategy: (1) chiral interactions occurring between chiral compounds and chiral matrices (“enantioselective interaction” strategy); and (2) recognizing sites inside molecular-imprinting polymers (MIPs; “key-to-lock” strategy). The chiral compounds of interest are not limited to chiral drugs, but also include other biologically important chiral compounds (e.g., amino acids). Based on our studies, this article reviews the state-of-the-art techniques and materials systems toward ESR. The emphasis is placed on the materials and material systems established for the ESR purpose." @default.
- W2365004724 created "2016-06-24" @default.
- W2365004724 creator A5007279852 @default.
- W2365004724 creator A5053410816 @default.
- W2365004724 creator A5058708429 @default.
- W2365004724 creator A5062753460 @default.
- W2365004724 creator A5073440172 @default.
- W2365004724 date "2016-05-23" @default.
- W2365004724 modified "2023-10-15" @default.
- W2365004724 title "Materials Established for Enantioselective Release of Chiral Compounds" @default.
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