Answers are grounded in this paper and cite their sources.
The S → N acylation rates of thioester functionalized coumarins on heptakis-[6-deoxy-6-(2-aminoethylsulfanyl)]-β-cyclodextrin were measured. A high yield of mono-acylation was achieved with products that form self-inclusion compounds. The differential fluorescence response of the functionalized cyclodextrins upon binding biomacromolecules shows the potential of the constructs as probes.
No takes yet. Share an insight, caveat, or question.
Gómez‐Biagi et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: