Fig. 6. Experimental ECD spectra of compounds 4 (black), and 7 (red) in MeOH. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)Published as part of Cao, Liang, Shehla, Nuzhat, Li, Bin, Jian, Yuqing, Peng, Caiyun, Sheng, Wenbing, Liu, Leping, Cai, Xiong, Man, Rongyong, Liao, Duan-Fang, Choudhary, M. Iqbal, Rahman, Atta-ur & Wang, Wei, 2020, Schinortriterpenoids from Tujia ethnomedicine Xuetong-The stems of Kadsura heteroclita, pp. 1-7 in Phytochemistry (112178) 169 on page 4, DOI: 10.1016/j.phytochem.2019.112178, http://zenodo.org/record/829366
Fig. 5. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 5. Experimental ECD spectrum of 5 (black) compared with the calculated ECD spectra of 5 (red) a...
Fig. 4. ECD spectra of compounds 1 and 2. ECD spectrum of 1 (black), calculated ECD spectra of 1 (da...
Fig. 7. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 3, 4, 5, 6.Published as part ...
Fig. 2. Structure of isolated compounds.Published as part of Cao, Liang, Shehla, Nuzhat, Li, Bin, Ji...
Fig. 3. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 1 or 2; Key NOESY () correlat...
Cao, Liang, Shehla, Nuzhat, Li, Bin, Jian, Yuqing, Peng, Caiyun, Sheng, Wenbing, Liu, Leping, Cai, X...
Fig. 5. X-ray crystallographic structure of 1.Published as part of Cao, Liang, Shehla, Nuzhat, Li, B...
Fig. 1. Characteristic NMR signals of SNTs (δC-10 = 96.0–99.9).Published as part of Cao, Liang, Sheh...
Fig. 4. Experimental CD spectrum (black lines) and calculated ECD spectra (red, green, and other lin...
Fig. 7. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 5. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 5. Experimental ECD spectrum of 5 (black) compared with the calculated ECD spectra of 5 (red) a...
Fig. 4. ECD spectra of compounds 1 and 2. ECD spectrum of 1 (black), calculated ECD spectra of 1 (da...
Fig. 7. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 3, 4, 5, 6.Published as part ...
Fig. 2. Structure of isolated compounds.Published as part of Cao, Liang, Shehla, Nuzhat, Li, Bin, Ji...
Fig. 3. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 1 or 2; Key NOESY () correlat...
Cao, Liang, Shehla, Nuzhat, Li, Bin, Jian, Yuqing, Peng, Caiyun, Sheng, Wenbing, Liu, Leping, Cai, X...
Fig. 5. X-ray crystallographic structure of 1.Published as part of Cao, Liang, Shehla, Nuzhat, Li, B...
Fig. 1. Characteristic NMR signals of SNTs (δC-10 = 96.0–99.9).Published as part of Cao, Liang, Sheh...
Fig. 4. Experimental CD spectrum (black lines) and calculated ECD spectra (red, green, and other lin...
Fig. 7. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 5. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 5. Experimental ECD spectrum of 5 (black) compared with the calculated ECD spectra of 5 (red) a...