Fig. 2. Selected HMBC correlations of compounds 2–7.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe, Wang, Zhenzhong & Xiao, Wei, 2020, Anti-inflammatory labdane diterpenoids from Leonurus japonicus Houtt, pp. 1-7 in Phytochemistry (112223) 173 on page 3, DOI: 10.1016/j.phytochem.2019.112223, http://zenodo.org/record/829461
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1, 3–5, 7, and 9.Published as part of Yu, ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 2. Key HMBC correlations of compounds 1–6.Published as part of Song, Zhuorui, Gao, Chengfeng, J...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 4. Comparison of experimental and calculated ECD spectra of 1–4 in MeOH.Published as part of Ya...
Fig. 1. Structures of compounds 1–10.Published as part of Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, K...
Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, Kai-Liang, Chen, Jian-Jun, Gao, Kun (2020): Halimane and la...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Fig. 2. 1 H–1 H COSY and key HMBC correlations of compounds 1 and 4–6.Published as part of Geng, Hao...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1, 3–5, 7, and 9.Published as part of Yu, ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 2. Key HMBC correlations of compounds 1–6.Published as part of Song, Zhuorui, Gao, Chengfeng, J...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 4. Comparison of experimental and calculated ECD spectra of 1–4 in MeOH.Published as part of Ya...
Fig. 1. Structures of compounds 1–10.Published as part of Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, K...
Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, Kai-Liang, Chen, Jian-Jun, Gao, Kun (2020): Halimane and la...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Fig. 2. 1 H–1 H COSY and key HMBC correlations of compounds 1 and 4–6.Published as part of Geng, Hao...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1, 3–5, 7, and 9.Published as part of Yu, ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 2. Key HMBC correlations of compounds 1–6.Published as part of Song, Zhuorui, Gao, Chengfeng, J...