Fig. 1. Structures of compounds 1–18.Published as part of Shu, Yan, Wang, Jia-Peng, Li, Bing-Xian, Gan, Jun-Li, Ding, Hao, Liu, Rui, Cai, Le & Ding, Zhong-Tao, 2022, Bioactive cytochalasans from the fungus Arthrinium arundinis DJ-13, pp. 1-8 in Phytochemistry (113009) 194 on page 2, DOI: 10.1016/j.phytochem.2021.113009, http://zenodo.org/record/823694
Fig. 1. Chemical structures of compounds 1–17.Published as part of Lin, Shuang, He, Yan, Li, Fengli,...
Fig. 3. The four possible diastereomers 1a-1d and the most populated conformer for each diastereomer...
Fig. 1. Structures of compounds 1–12.Published as part of Zhang, Xiao-Yan, Tan, Xiang-Mei, Yu, Meng,...
Shu, Yan, Wang, Jia-Peng, Li, Bing-Xian, Gan, Jun-Li, Ding, Hao, Liu, Rui, Cai, Le, Ding, Zhong-Tao ...
Fig. 4. X-ray crystal structure of 1, experimental and calculated ECD spectra of 2–6.Published as pa...
Fig. 3. Key NOE correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, Li, Bing-Xian, Ga...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, L...
Fig. 1. The chemical structures of compounds 1–14.Published as part of Gao, Suying, Wu, Ping, Xue, J...
Fig. 1. Chemical structure of asporychalasin (1).Published as part of Orfali, Raha, Perveen, Shaguft...
Fig. 1. Chemical structures of 1–13 isolated from C. africanus.Published as part of Yu, Muyuan, Kang...
Fig. 1. Structures of compounds 1–15.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, Wen-Ji...
Fig. 5. Proposed biosynthetic pathway for asporychalasin.Published as part of Orfali, Raha, Perveen,...
Fig. 13. The chemical structures of compounds 194–208 and 222-224.Published as part of Harneti, Desi...
Fig. 14. The chemical structures of compounds 209–221, and 225-248.Published as part of Harneti, Des...
Fig. 1. Structures of compounds 1–13.Published as part of Song, Jintong, Xu, Ke, Liu, Chunyu, Wang, ...
Fig. 1. Chemical structures of compounds 1–17.Published as part of Lin, Shuang, He, Yan, Li, Fengli,...
Fig. 3. The four possible diastereomers 1a-1d and the most populated conformer for each diastereomer...
Fig. 1. Structures of compounds 1–12.Published as part of Zhang, Xiao-Yan, Tan, Xiang-Mei, Yu, Meng,...
Shu, Yan, Wang, Jia-Peng, Li, Bing-Xian, Gan, Jun-Li, Ding, Hao, Liu, Rui, Cai, Le, Ding, Zhong-Tao ...
Fig. 4. X-ray crystal structure of 1, experimental and calculated ECD spectra of 2–6.Published as pa...
Fig. 3. Key NOE correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, Li, Bing-Xian, Ga...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, L...
Fig. 1. The chemical structures of compounds 1–14.Published as part of Gao, Suying, Wu, Ping, Xue, J...
Fig. 1. Chemical structure of asporychalasin (1).Published as part of Orfali, Raha, Perveen, Shaguft...
Fig. 1. Chemical structures of 1–13 isolated from C. africanus.Published as part of Yu, Muyuan, Kang...
Fig. 1. Structures of compounds 1–15.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, Wen-Ji...
Fig. 5. Proposed biosynthetic pathway for asporychalasin.Published as part of Orfali, Raha, Perveen,...
Fig. 13. The chemical structures of compounds 194–208 and 222-224.Published as part of Harneti, Desi...
Fig. 14. The chemical structures of compounds 209–221, and 225-248.Published as part of Harneti, Des...
Fig. 1. Structures of compounds 1–13.Published as part of Song, Jintong, Xu, Ke, Liu, Chunyu, Wang, ...
Fig. 1. Chemical structures of compounds 1–17.Published as part of Lin, Shuang, He, Yan, Li, Fengli,...
Fig. 3. The four possible diastereomers 1a-1d and the most populated conformer for each diastereomer...
Fig. 1. Structures of compounds 1–12.Published as part of Zhang, Xiao-Yan, Tan, Xiang-Mei, Yu, Meng,...