Fig. 3. The NOESY correlations of compounds of 1–7 and 9.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Liping, Yin, Jie, Li, Qin, Dai, Chong, Wang, Jianping, Gu, Lianghu, Tong, Qingyi, Zhu, Hucheng & Zhang, Yonghui, 2021, Spectanoids A H: Eight undescribed sesterterpenoids from Aspergillus spectabilis, pp. 1-10 in Phytochemistry (112910) 191 on page 6, DOI: 10.1016/j.phytochem.2021.112910, http://zenodo.org/record/825759
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Y...
Fig. 9. Structures of isopimaric-type diterpenoids 119–144.Published as part of Zhao, Wen-Yu, Yi, Ji...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–7 and 9.Published as part of Wei, Men...
Fig. 1. Structures of compounds 1–10.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Liping, Y...
Wei, Mengsha, Zhou, Peng, Huang, Liping, Yin, Jie, Li, Qin, Dai, Chong, Wang, Jianping, Gu, Lianghu,...
Fig. 4. X-ray crystallographic structures of compounds 1, 2 and 6.Published as part of Wei, Mengsha,...
Fig. 5. Experimental ECD spectra of 2 and 3.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Li...
Fig. 6. Proposed biosynthetical pathways of compounds 1–10.Published as part of Wei, Mengsha, Zhou, ...
Fig. 7. Compounds 3 and 6 induce apoptosis of human B lymphoma cells.Published as part of Wei, Mengs...
Fig. 3. Key NOE correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, Liu, Rui, Gan, Ju...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 15. Structures of other sesterterpenoids 208–213.Published as part of Zhao, Wen-Yu, Yi, Jing, C...
Fig. 7. Structures of other-type sesquiterpenoids 104–110.Published as part of Zhao, Wen-Yu, Yi, Jin...
Fig. 14. Structures of asperane-type sesterterpenoids 202–207.Published as part of Zhao, Wen-Yu, Yi,...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Y...
Fig. 9. Structures of isopimaric-type diterpenoids 119–144.Published as part of Zhao, Wen-Yu, Yi, Ji...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–7 and 9.Published as part of Wei, Men...
Fig. 1. Structures of compounds 1–10.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Liping, Y...
Wei, Mengsha, Zhou, Peng, Huang, Liping, Yin, Jie, Li, Qin, Dai, Chong, Wang, Jianping, Gu, Lianghu,...
Fig. 4. X-ray crystallographic structures of compounds 1, 2 and 6.Published as part of Wei, Mengsha,...
Fig. 5. Experimental ECD spectra of 2 and 3.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Li...
Fig. 6. Proposed biosynthetical pathways of compounds 1–10.Published as part of Wei, Mengsha, Zhou, ...
Fig. 7. Compounds 3 and 6 induce apoptosis of human B lymphoma cells.Published as part of Wei, Mengs...
Fig. 3. Key NOE correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, Liu, Rui, Gan, Ju...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 15. Structures of other sesterterpenoids 208–213.Published as part of Zhao, Wen-Yu, Yi, Jing, C...
Fig. 7. Structures of other-type sesquiterpenoids 104–110.Published as part of Zhao, Wen-Yu, Yi, Jin...
Fig. 14. Structures of asperane-type sesterterpenoids 202–207.Published as part of Zhao, Wen-Yu, Yi,...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Y...
Fig. 9. Structures of isopimaric-type diterpenoids 119–144.Published as part of Zhao, Wen-Yu, Yi, Ji...