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Beilstein J. Org. Chem. 2014, 10, 3111–3121, doi:10.3762/bjoc.10.328
Graphical Abstract
Figure 1: General structures of several D-glucose and D-glucosamine derivatives.
Scheme 1: Synthesis of amide and urea derivatives of the headgroup 3.
Figure 2: a) A translucent/opaque gel formed by compound 19 in EtOH/H2O (1:2) at 1.3 mg/mL; b) a gel formed b...
Figure 3: The rheological measurements of the gels formed by amide 11 (EtOH/H2O, 1:2) at 5.4 mg/mL, urea 16 (...
Figure 4: The optical micrographs of the wet gels formed by several amides. a) A gel formed by compound 8 in ...
Figure 5: The optical micrographs of the wet gel samples formed by several ureas. a) Compound 19 in DMSO/H2O ...
Figure 6: Stability test results under acidic conditions. a) A gel formed by compound 23 in DMSO/H2O (1:2) at...
Figure 7: Release of naproxen sodium from the gel formed by compound 16 to the aqueous phase.
Figure 8: Naproxen release study from the gel formed by compound 16 in the presence of acid.
Beilstein J. Org. Chem. 2011, 7, 234–242, doi:10.3762/bjoc.7.31
Figure 1: Structures of three ester derivatives of compound 1.
Figure 2: Structures of ester analogs 5–7 and headgroup 8.
Scheme 1: Synthesis of a series of esters 9A–18C.
Figure 3: Optical micrographs of the gels formed by compound 9A in hexane at 15 mg/mL (A, B), 9B in DMSO/wate...
Figure 4: An ethanol gel formed by compound 18A at <10 mg/mL. a) A clear solution when heated above 70 °C; b)...
Figure 5: Optical micrographs under bright field (a, b) and scanning electron micrograph (c) of the gel forme...
Figure 6: The UV–vis absorption spectra of the polymerized gel formed by compound 18A in ethanol (10 mg/mL): ...