Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, Aimin, Wei, Mengsha, Kang, Xin, Chen, Chunmei, Zhu, Hucheng & Zhang, Yonghui, 2022, 30-norlanostane triterpenoids and steroid derivatives from the endophytic fungus Aspergillus nidulans, pp. 1-8 in Phytochemistry (113257) 201 on page 4, DOI: 10.1016/j.phytochem.2022.113257, http://zenodo.org/record/823725
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 3. Key NOE correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, Liu, Rui, Gan, Ju...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
Fig. 1. Chemical structures of compounds 1–10.Published as part of Li, Qin, Zheng, Yuyi, Fu, Aimin, ...
Fig. 4. X-ray crystal structures of compounds 1 and 2.Published as part of Li, Qin, Zheng, Yuyi, Fu,...
Li, Qin, Zheng, Yuyi, Fu, Aimin, Wei, Mengsha, Kang, Xin, Chen, Chunmei, Zhu, Hucheng, Zhang, Yonghu...
Fig. 5. The experimental and calculated ECD spectra of compound 4.Published as part of Li, Qin, Zhen...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–7 and 9.Published as part of Wei, Men...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of neuropyrones A–E (1–5).Published as part of Li, X...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 3. Key NOE correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, Liu, Rui, Gan, Ju...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
Fig. 1. Chemical structures of compounds 1–10.Published as part of Li, Qin, Zheng, Yuyi, Fu, Aimin, ...
Fig. 4. X-ray crystal structures of compounds 1 and 2.Published as part of Li, Qin, Zheng, Yuyi, Fu,...
Li, Qin, Zheng, Yuyi, Fu, Aimin, Wei, Mengsha, Kang, Xin, Chen, Chunmei, Zhu, Hucheng, Zhang, Yonghu...
Fig. 5. The experimental and calculated ECD spectra of compound 4.Published as part of Li, Qin, Zhen...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–7 and 9.Published as part of Wei, Men...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of neuropyrones A–E (1–5).Published as part of Li, X...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 3. Key NOE correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, Liu, Rui, Gan, Ju...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...