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Beilstein J. Org. Chem. 2016, 12, 2883–2892, doi:10.3762/bjoc.12.287
Graphical Abstract
Scheme 1: Scheme for the end-capping of the PEG-NH2 (1)/α-CD pseudopolyrotaxane with 4-(azidomethyl)benzoic a...
Figure 1: SEC charts for crude products of reaction 1 (upper chart) and 2 (lower chart).
Figure 2: (A) SEC charts of α-CD, PEG-Ph-NH2 (3), PRX-Bn-N3 (4a), PRX-Ph-N3 (4b), and PRX-Ph-Me (4c). (B) FTI...
Scheme 2: End-group modification of 4a-c with model alkyne via copper-catalyzed click reaction.
Figure 3: (A) 1H NMR spectra of the PRXs before (4a, 4b, 4c) and after copper-catalyzed click reactions with p...
Scheme 3: Scheme of the synthesis of water-soluble PRX (6) and the following end group modification with copp...
Figure 4: SEC charts of the HEE-PRX-Bn-N3 (6) (A, B) and the HEE-PRX-DF488 (7) (C, D) monitored with fluoresc...
Figure 5: CLSM images of HeLa cells treated with HEE-PRX-DF488 (7) (500 μg/mL) for 26 h (scale bars: 20 μm). ...
Beilstein J. Org. Chem. 2014, 10, 2623–2629, doi:10.3762/bjoc.10.274
Scheme 1: Overall concept of the degradable PRX crosslinker.
Scheme 2: Overall reaction scheme of the resin monomer-soluble PRX crosslinker with degradable end groups.
Figure 1: 1H NMR spectrum of C12-Bu12 PRX (DMSO-d6).
Figure 2: 1H NMR spectrum of C12-Bu12-MA12 PRX (DMSO-d6).
Figure 3: SEC analysis of the prepared polymers a) PEG 10 k, b) C12-Bu12, c) C12-Bu12-MA12, d) C12-Bu12-MA12 ...
Figure 4: a) Image of the photosetting plastic prepared by resin casting and b) the results of the Vickers ha...