Fig. 3. Key NOESY correlations of compounds 1–9.Published as part of Cao, Zhen, Zhu, Shangjun, Xue, Zhaowei, Zhang, Fuxin, Zhang, Lei, Zhang, Yu, Guo, Yuting, Zhan, Guanqun, Zhang, Xinxin & Guo, Zengjun, 2022, Isoquinoline alkaloids from Hylomecon japonica and their potential anti-breast cancer activities, pp. 1-10 in Phytochemistry (113321) 202 on page 5, DOI: 10.1016/j.phytochem.2022.113321, http://zenodo.org/record/823579
Fig. 2. Key HMBC, COSY, and NOESY/ROESY correlations of hyphengshanols A–D (1–3 and 9).Published as ...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 3. Key NOESY (H→H) correlations of compounds 1–7.Published as part of Meng, Xian-Hua, Wang, Kai...
Fig. 2. Key HMBC (arrows) and 1H–1H COSY (bold) correlations of compounds 1–9.Published as part of C...
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.Published as part of Cao, Zhen, Zhu...
Cao, Zhen, Zhu, Shangjun, Xue, Zhaowei, Zhang, Fuxin, Zhang, Lei, Zhang, Yu, Guo, Yuting, Zhan, Guan...
Fig. 2. Key HMBC correlations of compound 1a/1b‒12.Published as part of Yin, Zhao-Kun, Liu, Zhao-Zhe...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–11.Published as part of Han, Yang, Hou, ...
Fig. 3. Key NOESY correlations of compounds 1, 4 and 6–11.Published as part of Han, Yang, Hou, Tao, ...
Fig. 2. Key COSY and HMBC correlations of compounds 1–6.Published as part of Zhang, Qin, Zan, Yan-Hu...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key HMBC and COSY correlations of aglycon and compounds 1–6.Published as part of Li, Fei, Wu...
Fig. 3. Key HMBC and COSY correlations of aglycon and compounds 1–6.Published as part of Li, Fei, Wu...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key HMBC, COSY, and NOESY/ROESY correlations of hyphengshanols A–D (1–3 and 9).Published as ...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 3. Key NOESY (H→H) correlations of compounds 1–7.Published as part of Meng, Xian-Hua, Wang, Kai...
Fig. 2. Key HMBC (arrows) and 1H–1H COSY (bold) correlations of compounds 1–9.Published as part of C...
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.Published as part of Cao, Zhen, Zhu...
Cao, Zhen, Zhu, Shangjun, Xue, Zhaowei, Zhang, Fuxin, Zhang, Lei, Zhang, Yu, Guo, Yuting, Zhan, Guan...
Fig. 2. Key HMBC correlations of compound 1a/1b‒12.Published as part of Yin, Zhao-Kun, Liu, Zhao-Zhe...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–11.Published as part of Han, Yang, Hou, ...
Fig. 3. Key NOESY correlations of compounds 1, 4 and 6–11.Published as part of Han, Yang, Hou, Tao, ...
Fig. 2. Key COSY and HMBC correlations of compounds 1–6.Published as part of Zhang, Qin, Zan, Yan-Hu...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key HMBC and COSY correlations of aglycon and compounds 1–6.Published as part of Li, Fei, Wu...
Fig. 3. Key HMBC and COSY correlations of aglycon and compounds 1–6.Published as part of Li, Fei, Wu...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key HMBC, COSY, and NOESY/ROESY correlations of hyphengshanols A–D (1–3 and 9).Published as ...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 3. Key NOESY (H→H) correlations of compounds 1–7.Published as part of Meng, Xian-Hua, Wang, Kai...