Fig. 3. Key NOESY/ROESY correlations of compounds 1, 2, 4, 7, 9–11, and 13.Published as part of Sun, Mo-Han, Ma, Xian-Jie, Shao, Si-Yuan, Han, Shao-Wei, Jiang, Jian-Wei, Zhang, Jian-Jun & Li, Shuai, 2021, Phenanthrene, 9,10-dihydrophenanthrene and bibenzyl enantiomers from Bletilla striata with their antineuroinflammatory and cytotoxic activities, pp. 1-14 in Phytochemistry (112609) 182 on page 5, DOI: 10.1016/j.phytochem.2020.112609, http://zenodo.org/record/829142
Abstract − Column chromatographic separation of the MeOH extract from the tubers of Bletilla striata...
Fig. 5. Correlation coefficients and DP4+ analysis between experimental and calculated 13C NMR chemi...
Fig. 3. The key NOESY correlations of cyclohexenyl unit of 5 9.Published as part of Nguyen, Mai T.T....
Fig. 2. Key HMBC (→) and COSY (bold) correlations of compounds 1, 2, 4, 7, 9, 11 and 13.Published as...
Fig. 1. Structures of compounds 1–25.Published as part of Sun, Mo-Han, Ma, Xian-Jie, Shao, Si-Yuan, ...
Sun, Mo-Han, Ma, Xian-Jie, Shao, Si-Yuan, Han, Shao-Wei, Jiang, Jian-Wei, Zhang, Jian-Jun, Li, Shuai...
Fig. 5. Plausible Biogenetic Pathway of Compounds 1–13.Published as part of Sun, Mo-Han, Ma, Xian-Ji...
Fig. 2. Key 2D NMR correlations of compounds 1, 3, 6, and 8.Published as part of Zhou, Ming, Yuan, F...
Fig. 3. Key 2D NMR correlations of compound 12.Published as part of Zhou, Ming, Yuan, Fang, Ruan, Ha...
Fig. 2. Key HMBC correlations of compounds 1–6.Published as part of Cheng, Zhuo-Yang, Zhang, Ding-Di...
Fig. 3. Key ROESY correlations for compounds 6 and 9.Published as part of Quan, Li-Qiu, Hegazy, Ahme...
Fig. 3. Key NOESY correlations of compounds 1, and 3–6.Published as part of Cheng, Zhuo-Yang, Zhang,...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. 1H– 1H COSY correlations for compounds 6–10 and key HMBC correlations for compounds 1 and 6–...
Fig. 3. Key NOESY correlations for 1, 3/4, 10, and 13.Published as part of Youn, Isoo, Han, Kyu-Yeon...
Abstract − Column chromatographic separation of the MeOH extract from the tubers of Bletilla striata...
Fig. 5. Correlation coefficients and DP4+ analysis between experimental and calculated 13C NMR chemi...
Fig. 3. The key NOESY correlations of cyclohexenyl unit of 5 9.Published as part of Nguyen, Mai T.T....
Fig. 2. Key HMBC (→) and COSY (bold) correlations of compounds 1, 2, 4, 7, 9, 11 and 13.Published as...
Fig. 1. Structures of compounds 1–25.Published as part of Sun, Mo-Han, Ma, Xian-Jie, Shao, Si-Yuan, ...
Sun, Mo-Han, Ma, Xian-Jie, Shao, Si-Yuan, Han, Shao-Wei, Jiang, Jian-Wei, Zhang, Jian-Jun, Li, Shuai...
Fig. 5. Plausible Biogenetic Pathway of Compounds 1–13.Published as part of Sun, Mo-Han, Ma, Xian-Ji...
Fig. 2. Key 2D NMR correlations of compounds 1, 3, 6, and 8.Published as part of Zhou, Ming, Yuan, F...
Fig. 3. Key 2D NMR correlations of compound 12.Published as part of Zhou, Ming, Yuan, Fang, Ruan, Ha...
Fig. 2. Key HMBC correlations of compounds 1–6.Published as part of Cheng, Zhuo-Yang, Zhang, Ding-Di...
Fig. 3. Key ROESY correlations for compounds 6 and 9.Published as part of Quan, Li-Qiu, Hegazy, Ahme...
Fig. 3. Key NOESY correlations of compounds 1, and 3–6.Published as part of Cheng, Zhuo-Yang, Zhang,...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. 1H– 1H COSY correlations for compounds 6–10 and key HMBC correlations for compounds 1 and 6–...
Fig. 3. Key NOESY correlations for 1, 3/4, 10, and 13.Published as part of Youn, Isoo, Han, Kyu-Yeon...
Abstract − Column chromatographic separation of the MeOH extract from the tubers of Bletilla striata...
Fig. 5. Correlation coefficients and DP4+ analysis between experimental and calculated 13C NMR chemi...
Fig. 3. The key NOESY correlations of cyclohexenyl unit of 5 9.Published as part of Nguyen, Mai T.T....