Fig. 3. X-ray ORTEP drawings of compounds 1, 3, 6, and 8.Published as part of Zhou, Peng, Zheng, Meijia, Li, Xiao-Nian, Wei, Mengsha, Zhang, Mi, Li, Qin, Zang, Yi, Sun, Weiguang, Wang, Jianping, Zhu, Hucheng, Chen, Chunmei & Zhang, Yonghui, 2021, Hypoxylonoids A G: Isopimarane diterpene glycosides from Xylaria hypoxylon, pp. 1-9 in Phytochemistry (112613) 182 on page 5, DOI: 10.1016/j.phytochem.2020.112613, http://zenodo.org/record/829140
Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Fig. 4. ORTEP drawing of pierisjapanoside B (2).Published as part of Zheng, Guijuan, Jin, Pengfei, H...
Fig. 1. Structures of compounds 1–12.Published as part of Zhou, Peng, Zheng, Meijia, Li, Xiao-Nian, ...
Zhou, Peng, Zheng, Meijia, Li, Xiao-Nian, Wei, Mengsha, Zhang, Mi, Li, Qin, Zang, Yi, Sun, Weiguang,...
Fig. 4. Key NOESY correlations of compounds 2, 4, 5, and 7.Published as part of Zhou, Peng, Zheng, M...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 5. Experimental ECD spectra of compounds 1–8 in MeOH.Published as part of Zhou, Peng, Zheng, Me...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 1. Structures of compounds 1–12 isolated from Euphorbia neriifolia.Published as part of Li, Jia...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 3. ORTEP drawings of compounds 1, 3 and 5.Published as part of Zhao, Yan-rong, Zou, Guo-an & Ai...
Fig. 3. ORTEP drawing for compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 3. ORTEP drawing of pierisjapanoside A (1).Published as part of Zheng, Guijuan, Jin, Pengfei, H...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Fig. 4. ORTEP drawing of pierisjapanoside B (2).Published as part of Zheng, Guijuan, Jin, Pengfei, H...
Fig. 1. Structures of compounds 1–12.Published as part of Zhou, Peng, Zheng, Meijia, Li, Xiao-Nian, ...
Zhou, Peng, Zheng, Meijia, Li, Xiao-Nian, Wei, Mengsha, Zhang, Mi, Li, Qin, Zang, Yi, Sun, Weiguang,...
Fig. 4. Key NOESY correlations of compounds 2, 4, 5, and 7.Published as part of Zhou, Peng, Zheng, M...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 5. Experimental ECD spectra of compounds 1–8 in MeOH.Published as part of Zhou, Peng, Zheng, Me...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 1. Structures of compounds 1–12 isolated from Euphorbia neriifolia.Published as part of Li, Jia...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 3. ORTEP drawings of compounds 1, 3 and 5.Published as part of Zhao, Yan-rong, Zou, Guo-an & Ai...
Fig. 3. ORTEP drawing for compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 3. ORTEP drawing of pierisjapanoside A (1).Published as part of Zheng, Guijuan, Jin, Pengfei, H...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Fig. 4. ORTEP drawing of pierisjapanoside B (2).Published as part of Zheng, Guijuan, Jin, Pengfei, H...