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Beilstein J. Org. Chem. 2017, 13, 1893–1899, doi:10.3762/bjoc.13.184
Graphical Abstract
Scheme 1: Nucleophilic substitution of the 4-toluenesulfonyl group. The formalism for the mechanochemical act...
Figure 1: Effect of jar size on the reaction time using an equal number (30) of steel balls (ø 1 mm) for the ...
Figure 2: Effect of ball size on the reaction time to a full conversion of Ts-β-CD: a) reactions performed at...
Figure 3: Reaction time as a function of ball materials at 550 min−1 in glass vials of 25 mL: a) equal weight...
Beilstein J. Org. Chem. 2014, 10, 3007–3018, doi:10.3762/bjoc.10.319
Scheme 1: Schematic representation of the various synthetic routes for the introduction of an anchoring group...
Scheme 2: Synthetic strategy for the rhodaminylation of β-CD polymer.
Figure 1: TLC study of β-CD iodination showing the proceeding of 6-monoiodination with increasing reaction ti...
Figure 2: HSQC-DEPT spectrum of compound 1 with partial assignment.
Figure 3: IR spectra of compound 1 (black line) and compound 2 (red line) showing the disappearance of the az...
Scheme 3: Schematic representation for the coumarinylation of methylated β-CD-polymer, n, m, p and q mean the...
Figure 4: HSQC-DEPT spectra of compound 4 with partial assignment; in the upper part the full spectrum is sho...
Scheme 4: Schematic representation for the introduction of NBF in a cationic β-CD-polymer.
Scheme 5: Schematic representation for the introduction of fluorescein into a β-CD-polymer.
Beilstein J. Org. Chem. 2014, 10, 2836–2843, doi:10.3762/bjoc.10.301
Figure 1: Aggregate size analysis of aqueous solutions of G8 and ibuprofen by PCS. a) G8 in 1% solution; b) s...
Scheme 1: Schematic representation of the preparation of HP-substituted maltooligomers.
Figure 2: Electropherograms of tested model drugs in the presence of 2-hydroxypropylated acyclic and cyclic d...