Fig. 2. Structures of the identified compounds. For the compounds 5–7 and 36, only the relative configuration is given. Tentatively identified compounds are labeled with an asterisk.Published as part of Or, Dejan, ci, c, Bere, Sanja, zni, Du, Skori, san, c & Mimica-Dukic, Neda, 2021, Comprehensive study of Anthriscus sylvestris lignans, pp. 1-22 in Phytochemistry (112958) 192 on page 3, DOI: 10.1016/j.phytochem.2021.112958, http://zenodo.org/record/825813
Fig. 1. Structures of compounds 1-23.Published as part of Huang, Ya-Ping, Zhao, Yuan-Yu, Johnson, Ol...
Fig. 1. Structures of compounds 1–8.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guan...
Fig. 1. Structures of compounds 1–19.Published as part of Ablajan, Nurfida, Zhao, Bo, Zhao, Jiang-Yu...
Fig. 5. Unsaturated dibenzylbutyrolactones and aryltetralins fragmentation (based on Schmidt et al.,...
Fig. 6. Saturated dibenzylbutyrolactones fragmentation (based on Eklund et al., 2008; Schmidt et al....
Fig. 7. Proposed 8-hydroxydibenzylbutyrolactones fragmentation (based on Crotti et al., 2004; Schmid...
Fig. 8. 7-hydroxy and 7-acyloxyaryltetralin fragmentation (based on Chen et al., 1985; Vasilev et al...
Or, Dejan, ci, c, Bere, Sanja, zni, Du, Skori, san, c, Mimica-Dukic, Neda (2021): Comprehensive stud...
Fig. 3. Comparison of UV spectra of class representatives.Published as part of Or, Dejan, ci, c, Ber...
Fig. 1. Positive- and negative-ion mass chromatograms and extracted wavelength chromatogram (300 ± 4...
The aryltetralin lignan deoxypodophyllotoxin is much more widespread in the plant kingdom than podop...
Fig. 4. Comparison of positive-ionization MS2 spectra of class representatives at V = 10 V.Published...
Fig. 1. Chemical structures of compounds 1–12.Published as part of Mo, Shuyuan, Yin, Jie, Ye, Zi, Li...
Fig. 1. Chemical structures of novel compounds1-16.Published as part of Meng, FanCheng, Ma, YingXion...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Shi, Zhengyi, Tan, Xiaosheng, Hu, ...
Fig. 1. Structures of compounds 1-23.Published as part of Huang, Ya-Ping, Zhao, Yuan-Yu, Johnson, Ol...
Fig. 1. Structures of compounds 1–8.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guan...
Fig. 1. Structures of compounds 1–19.Published as part of Ablajan, Nurfida, Zhao, Bo, Zhao, Jiang-Yu...
Fig. 5. Unsaturated dibenzylbutyrolactones and aryltetralins fragmentation (based on Schmidt et al.,...
Fig. 6. Saturated dibenzylbutyrolactones fragmentation (based on Eklund et al., 2008; Schmidt et al....
Fig. 7. Proposed 8-hydroxydibenzylbutyrolactones fragmentation (based on Crotti et al., 2004; Schmid...
Fig. 8. 7-hydroxy and 7-acyloxyaryltetralin fragmentation (based on Chen et al., 1985; Vasilev et al...
Or, Dejan, ci, c, Bere, Sanja, zni, Du, Skori, san, c, Mimica-Dukic, Neda (2021): Comprehensive stud...
Fig. 3. Comparison of UV spectra of class representatives.Published as part of Or, Dejan, ci, c, Ber...
Fig. 1. Positive- and negative-ion mass chromatograms and extracted wavelength chromatogram (300 ± 4...
The aryltetralin lignan deoxypodophyllotoxin is much more widespread in the plant kingdom than podop...
Fig. 4. Comparison of positive-ionization MS2 spectra of class representatives at V = 10 V.Published...
Fig. 1. Chemical structures of compounds 1–12.Published as part of Mo, Shuyuan, Yin, Jie, Ye, Zi, Li...
Fig. 1. Chemical structures of novel compounds1-16.Published as part of Meng, FanCheng, Ma, YingXion...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Shi, Zhengyi, Tan, Xiaosheng, Hu, ...
Fig. 1. Structures of compounds 1-23.Published as part of Huang, Ya-Ping, Zhao, Yuan-Yu, Johnson, Ol...
Fig. 1. Structures of compounds 1–8.Published as part of Xu, Ce, Xu, Kuo, Yuan, Xiao-Long, Ren, Guan...
Fig. 1. Structures of compounds 1–19.Published as part of Ablajan, Nurfida, Zhao, Bo, Zhao, Jiang-Yu...