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Beilstein J. Org. Chem. 2023, 19, 889–891, doi:10.3762/bjoc.19.66
Beilstein J. Org. Chem. 2016, 12, 29–42, doi:10.3762/bjoc.12.5
Graphical Abstract
Figure 1: Chemical structures, logP values and molecular volumes (V) of carvacrol (1) and thymol (2). ahttp:/...
Figure 2: Phase solubility profiles of (a) CD/carvacrol (1) and (b) CD/thymol (2) inclusion complexes. Inset:...
Figure 3: 2D DOSY NMR spectra of (a) β-CD, carvacrol (1) and β-CD/carvacrol (1) inclusion complex and (b) β-C...
Figure 4: Representation of chemical shifts variations (Δδ) of a) carvacrol (1) and c) thymol (2) protons and...
Figure 5: 2D ROESY plots of β-CD/carvacrol (1) complex in D2O showing the NOEs between the H-3 and H-5 proton...
Figure 6: 2D ROESY plots of β-CD/thymol (2) complex in D2O showing the NOEs between the H-3 and H-5 protons o...
Figure 7: Representation of the most stable CD/guest inclusion complex conformers.
Figure 8: Effects of β-CD and HP-β-CD on the TEAC (μmol Trolox/ g of guest) of carvacrol (1) and thymol (2) b...
Beilstein J. Org. Chem. 2014, 10, 2322–2331, doi:10.3762/bjoc.10.241
Figure 1: Chemical structure of studied phenylpropanoids (PPs).
Figure 2: Phase solubility profiles of (a) CD/trans-anethole and (b) CD/p-coumaric acid inclusion complexes.
Figure 3: Solubility enhancement (log (St/S0)) as a function of the solubility (log (S0)) of studied phenylpr...
Figure 4: Representation of the most stable CD/trans-anethole inclusion complex conformers resulting from the...
Figure 5: DPPH radical scavenging activity (%) of studied PPs alone or in presence of CD.