This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2017, 13, 417–427, doi:10.3762/bjoc.13.45
Graphical Abstract
Figure 1: Structures of G agents.
Figure 2: Scavenger based on a heterodifunctionalized β-cyclodextrin derivative.
Figure 3: Structures of β-cyclodextrin derivatives 2–5.
Figure 4: Structures of pesticides tested.
Scheme 1: Synthetic pathway to derivatives 2 and 3 (Tr = trityl).
Scheme 2: Synthesis of compound 4.
Scheme 3: Synthesis of compound 5 (Tr = trityl).
Figure 5: Hydrolysis of methyl paraoxon (0.5 mM) in the presence of compounds 1, 2, 3 or 2-iodosobenzoic acid...
Figure 6: Hydrolysis of methyl paraoxon (0.5 mM) in the presence of compounds 1, 2, 3 or 2-iodosobenzoic acid...
Figure 7: Hydrolysis of methyl paraoxon (0.5 mM) in the presence of compounds 2, 4, 5 or 2-iodosobenzoic acid...
Figure 8: Hydrolysis of methyl paraoxon (0.5 mM) in the presence of mixtures of compounds 4, 5 with IBA or im...
Figure 9: Influence of the pesticide structure on the hydrolytic efficiency of compound 2 (0.25 mM). Kinetic ...
Figure 10: Influence of TRIMEB, IBA and imidazole on the hydrolysis of methyl parathion (0.5 mM). The final co...
Figure 11: Ability of compounds 1–4 in preventing the inhibition of acetylcholinesterase by soman (GD).
Beilstein J. Org. Chem. 2016, 12, 204–228, doi:10.3762/bjoc.12.23
Figure 1: Structure of NOPs.
Figure 2: Examples of structures of NOPs.
Figure 3: Structures of pesticides studied in the literature as guest to form an inclusion complex with CDs.
Figure 4: Structures of pesticides sensitive to the presence of CDs.
Scheme 1: The hydrolysis mechanism of substrate (S) in presence of a cyclodextrin (CD).
Figure 5: Structures of the different stereoisomers of G agents.
Scheme 2: Reaction mechanism of CD accelerated decomposition of organophosphorus compound (PX).
Scheme 3: Proposed degradation mechanism of cyclosarin by β-CD [72].
Figure 6: Schematic representations of β-CD and TRIMEB.
Scheme 4: Synthetic pathways to 6-monosubstituted CD derivatives.
Scheme 5: Synthetic pathways to 2-monosubstituted CD by an iodosobenzoate group.
Scheme 6: Synthetic pathways to 2-monosubstituted CDs with N–OH derivatives.
Scheme 7: Synthetic pathways to 3-monosubstituted CDs.
Scheme 8: Synthetic pathways to 3-homodisubstituted CDs.
Scheme 9: Synthetic pathways to 2,3-heterodisubstituted CDs.