A general high-yielding method for the preparation of monosubstituted β-cyclodextrin derivatives which have attached a thiol group in position 6 is described. The thiol group is attached through linkers of different lengths and repeating units (ethylene glycol or methylene). The target compounds were characterized by IR, MS and NMR spectra. A simple method for their complete conversion to the corresponding disulfides as well as a method for the reduction of the disulfides back to the thiols is presented. Both, thiols and disulfides are derivatives usable for well-defined covalent attachment of cyclodextrin to gold or polydopamine-coated solid surfaces.

Department of Organic Chemistry Faculty of Science Charles University Prague Hlavova 8 128 43 Prague 2 Czech Republic

Department of Teaching and Didactics of Chemistry Faculty of Science Charles University Prague Hlavova 8 128 43 Prague 2 Czech Republic

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Continuous flow synthesis of 6-monoamino-6-monodeoxy-β-cyclodextrin

Mono-6-Substituted Cyclodextrins-Synthesis and Applications