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Acyclic Cucurbituril Featuring Pendant Cyclodextrins
We report the design and synthesis of the acyclic cucurbit[n]uril–β-cyclodextrin chimeric host H1. The goal of the study is to deepen the cavity of the receptor to allow β-CD complexation of moieties on the guest (especially fentanyl) that protrude from the cavity of the primary acyclic CB[n] bindin...
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| Pubblicato in: | Supramol Chem |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8294166/ https://ncbi.nlm.nih.gov/pubmed/34305377 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/10610278.2021.1927033 |
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