Fig. 4. Comparison of experimental and calculated ECD spectra of 1–4 in MeOH.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 5, DOI: 10.1016/j.phytochem.2019.112223, http://zenodo.org/record/829461
Fig. 6. Experimental electronic circular dichroism (ECD) spectra of 1 and 3–6.Published as part of S...
Fig. 6. Experimental and calculated ECD spectra of 3 (A) and experimental ECD curves of compounds 3 ...
Fig. 4. Experimental and calculated ECD spectra for 1–6.Published as part of Singha, Suriphon, Yotma...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 2. Selected HMBC correlations of compounds 2–7.Published as part of Yang, Biao, Hu, Yumei, Chen...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
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. 5. Experimental and calculated ECD spectra of compound 4 (in MeOH).Published as part of Yu, Zha...
Fig. 4. Experimental and calculated ECD spectra of 1 (A) and experimental ECD curves of compounds 1 ...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 6. Experimental electronic circular dichroism (ECD) spectra of 1 and 3–6.Published as part of S...
Fig. 6. Experimental and calculated ECD spectra of 3 (A) and experimental ECD curves of compounds 3 ...
Fig. 4. Experimental and calculated ECD spectra for 1–6.Published as part of Singha, Suriphon, Yotma...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 2. Selected HMBC correlations of compounds 2–7.Published as part of Yang, Biao, Hu, Yumei, Chen...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
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. 5. Experimental and calculated ECD spectra of compound 4 (in MeOH).Published as part of Yu, Zha...
Fig. 4. Experimental and calculated ECD spectra of 1 (A) and experimental ECD curves of compounds 1 ...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 6. Experimental electronic circular dichroism (ECD) spectra of 1 and 3–6.Published as part of S...
Fig. 6. Experimental and calculated ECD spectra of 3 (A) and experimental ECD curves of compounds 3 ...
Fig. 4. Experimental and calculated ECD spectra for 1–6.Published as part of Singha, Suriphon, Yotma...