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Beilstein J. Org. Chem. 2020, 16, 1732–1739, doi:10.3762/bjoc.16.145
Graphical Abstract
Figure 1: Chemical structures of MPD and the three structural analogs MPC-1, MPC-2, and MPC-3. The molecular ...
Figure 2: Chemical structures of commercially available (S)-citronellol (Cit), 4,4′-dihydroxybenzophenone (BZ...
Figure 3: The synthetic route leading to compounds MPC-1 and MPC-2. Compound β-4Ac-Man-CEP was prepared in 4 ...
Figure 4: Preparation of mannosyl phosphoramidites. Starting from 2,3,4,6-tetra-O-acetyl-β-ᴅ-mannopyranose (β...
Beilstein J. Org. Chem. 2014, 10, 1589–1595, doi:10.3762/bjoc.10.164
Figure 1: (A) Structures of 1,8-dialkynylpyrene (Y) and PDI (E); (B) illustration of the electrostatic potent...
Figure 2: A plot of melting temperature (Tm) versus the number of pyrene–PDI interactions for duplexes 1*2 to ...
Figure 3: UV–vis absorption spectra (scaled) of duplexes 1*2 (blue) and 1*6 (red) at 20 °C. Conditions: see Table 1.
Figure 4: UV–vis absorption spectra (scaled) of duplexes 1*2 to 1*6 at 20 °C. Conditions: see Table 1.
Figure 5: Temperature-dependent UV–vis absorption spectrum of 1*2. Conditions: see Table 1.
Figure 6: Fluorescence spectra of oligomer 1 (black), duplex 1*2 (blue) and duplex 1*6 (red) at 20 °C. Excita...
Figure 7: PAGE experiment. All oligomers were used in a total amount of 150 pmol in 10 mM sodium phosphate bu...