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Beilstein J. Org. Chem. 2019, 15, 695–702, doi:10.3762/bjoc.15.64
Graphical Abstract
Figure 1: Structures of compounds 1–8.
Figure 2: 1H,1H COSY and key HMBC correlations of compounds 1–4 and 6.
Figure 3: Key NOESY correlations for compounds 1–4 and 6.
Beilstein J. Org. Chem. 2013, 9, 908–917, doi:10.3762/bjoc.9.104
Scheme 1: The structures of the NSAIDs and peptides explored as the building blocks of hydrogelators in this ...
Scheme 2: The synthetic route of the naproxen-containing hydrogelators and the corresponding precursors: (i) ...
Figure 1: Optical images of the hydrogels formed by (A) 1a (0.8 wt %, pH 7.0); (B) 1b (0.8 wt %, pH 4.0); (C) ...
Figure 2: The TEM images of the matrices of the hydrogels formed by (A) 1a (0.8 wt %, pH 7.0); (B) 1b (0.8 wt...
Figure 3: Recovery of the storage moduli of the gels formed by 0.8 wt % of 1a at pH 7.0 and 1.5 wt % of 1d fo...
Figure 4: The IC50 values of 1a, 1c and 1d incubated with HeLa cells after 72 h.
Beilstein J. Org. Chem. 2011, 7, 167–172, doi:10.3762/bjoc.7.23
Scheme 1: The chemical structures of the phenylalanine derivatives.
Figure 1: Optical images of (A) gel IV (1.5 wt %, pH = 4.6), (B) gel IV after UV irradiation (no aging), (C) ...
Figure 2: The optical images of (A) solution of 6 (2 wt %, pH = 9.0), (B) suspension of 6 (2 wt %, pH = 6.5),...
Figure 3: (A) Frequency dependence of dynamic storage modulus (G’) and loss modulus (G”) of gels I to IV at 1...
Figure 4: TEM images of the nanofibers that act as the matrices of gel I (A), gel II (B), gel III (C) and gel ...
Figure 5: The emission spectra (slit width = 3.0 nm) of the gels I–III and their solutions (I: λex= 265 nm; II...