2024
DOI: 10.1016/j.phytochem.2023.113933
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Four pairs of neolignan enantiomers with distinctive isochroman moiety from the fruits of Crataegus pinnatifida and their protective activities against H2O2-induced SH-SY5Y cells

Peng Zhao,
Shi-Fang Li,
Jiao-Yang Hou
et al.
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Cited by 2 publications
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“…Analysis of the calculated and experimental 13 C NMR data revealed that the relative configuration of 1 was 2″S,3″S with a DP4+ probability of 99.88% (Figure 5 and Tables S2−S11). 39 At the same time, the calculated data of the two isomers (2″S,3″S) and (2″R,3″R) and the experimental 13 C NMR chemical shifts of compound 1 were subjected to regression analysis. Among them, the structure (2″S,3″S) showed a better matching value of R 2 of 0.9986 (Figure 5).…”
Section: ■ Introductionmentioning
confidence: 99%
“…Analysis of the calculated and experimental 13 C NMR data revealed that the relative configuration of 1 was 2″S,3″S with a DP4+ probability of 99.88% (Figure 5 and Tables S2−S11). 39 At the same time, the calculated data of the two isomers (2″S,3″S) and (2″R,3″R) and the experimental 13 C NMR chemical shifts of compound 1 were subjected to regression analysis. Among them, the structure (2″S,3″S) showed a better matching value of R 2 of 0.9986 (Figure 5).…”
Section: ■ Introductionmentioning
confidence: 99%