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Beilstein J. Org. Chem. 2011, 7, 173–178, doi:10.3762/bjoc.7.24
Graphical Abstract
Figure 1: Examples of azole derivatives as important therapeutic agents.
Scheme 1: Michael-type addition of azoles of broad-scale acidity 1a–h to methyl acrylate (2) under basic cond...
Scheme 2: Chemical evidence for a regioselective Michael-type addition of 4(5)-nitroimidazole (1c) to methyl ...
Beilstein J. Org. Chem. 2010, 6, No. 34, doi:10.3762/bjoc.6.34
Figure 1: Examples of symmetrical and unsymmetrical α,ω-nucleobase amide-conjugated systems.
Scheme 1: Synthesis of main acidic subunits, precursors of both symmetrical and unsymmetrical α,ω-nucleobase ...
Figure 2: X-ray structure of 1ea shown as thermal ellipsoids at 50% probability [17,18].
Figure 3: DMT-MM in its presumably more stable conformation [20].
Figure 4: TEM images of symmetrical α,ω-nucleobase amide-conjugated systems: A – two splitting nucleoside nan...
Figure 5: Models of micro- and nanofibres based on hydrogen bonding interactions between thymine units; (A) t...
Beilstein J. Org. Chem. 2007, 3, No. 40, doi:10.1186/1860-5397-3-40
Scheme 1: Michael-type addition of 5-substituted uracil derivatives to 2-hydroxyethyl acrylate.
Scheme 2: Synthesis of the model ester-conjugated acyclic nucleoside.
Figure 1: Protons assignment in NMR spectrum of the model ester-conjugated nucleoside (4).