Fig. 4. Unequivocally established stereostructures of cyclocuparanols found in M. polymorpha in this work.Published as part of Zlatkovi, Dragan B., c, Đorđevic, Miljana R., Zlatkovi, c & Radulovic, Niko S., 2023, On the configuration and occurrence of 2,6-cyclocuparan-3-ols: Resolving a lasting discrepancy, pp. 1-10 in Phytochemistry (113566) 207 on page 5, DOI: 10.1016/j.phytochem.2022.113566, http://zenodo.org/record/829050
Fig. 1. Chemical structures of compounds 1–11.Published as part of Pei, Yue-Hu, Zhang, Li-Hua, Wu, X...
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).P...
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.Published as part of Yan, Wei, Ji, Wenxia, Ping, ...
Zlatkovi, Dragan B., c, Đorđevic, Miljana R., Zlatkovi, c, Radulovic, Niko S. (2023): On the configu...
Fig. 1. Structures of diastereomeric cyclocuparanols as reported in the literature. The carbon numbe...
Fig. 2. Cuparene compounds structurally related to 1–4.Published as part of Zlatkovi, Dragan B., c, ...
Fig. 3. a) MeLi, yield: 98% (Srikrishna and Ramachary, 2007); b) Ph3PCH2, 91% (Srikrishna and Ramach...
Fig. 5. MM2 molecular models of cyclocuparanol (3), microbiotol (4), and grimaldone (7A); 7B is the ...
Fig. 7. Dehydration and aromatization of compounds 1–4.Published as part of Zlatkovi, Dragan B., c, ...
Fig. 6. IR fingerprint regions of cyclopropane cuparenols 1–4, isolated in this work, and structural...
Fig. 6. ECD comparison in CH3CN. A: tricyclic bergamotanes (compounds 1, 5, 6, 9 and 10). B: bicycli...
Fig. 8. The "rear" Octant projections as viewed along double-bond axis for sporulaminals A and B pre...
Fig. 6. Mass spectrum of the prenyl crotonate peak from a Macrozamia miquelii pollen cone sample (Th...
Fig. 2. The key HMBC correlations of 1 8.Published as part of Pei, Yue-Hu, Zhang, Li-Hua, Wu, Xi-Le,...
Fig. 7. The Mo2(OAc)4 induced circular dichroism (ICD) spectrum of compound 3a in anhydrous DMSO wit...
Fig. 1. Chemical structures of compounds 1–11.Published as part of Pei, Yue-Hu, Zhang, Li-Hua, Wu, X...
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).P...
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.Published as part of Yan, Wei, Ji, Wenxia, Ping, ...
Zlatkovi, Dragan B., c, Đorđevic, Miljana R., Zlatkovi, c, Radulovic, Niko S. (2023): On the configu...
Fig. 1. Structures of diastereomeric cyclocuparanols as reported in the literature. The carbon numbe...
Fig. 2. Cuparene compounds structurally related to 1–4.Published as part of Zlatkovi, Dragan B., c, ...
Fig. 3. a) MeLi, yield: 98% (Srikrishna and Ramachary, 2007); b) Ph3PCH2, 91% (Srikrishna and Ramach...
Fig. 5. MM2 molecular models of cyclocuparanol (3), microbiotol (4), and grimaldone (7A); 7B is the ...
Fig. 7. Dehydration and aromatization of compounds 1–4.Published as part of Zlatkovi, Dragan B., c, ...
Fig. 6. IR fingerprint regions of cyclopropane cuparenols 1–4, isolated in this work, and structural...
Fig. 6. ECD comparison in CH3CN. A: tricyclic bergamotanes (compounds 1, 5, 6, 9 and 10). B: bicycli...
Fig. 8. The "rear" Octant projections as viewed along double-bond axis for sporulaminals A and B pre...
Fig. 6. Mass spectrum of the prenyl crotonate peak from a Macrozamia miquelii pollen cone sample (Th...
Fig. 2. The key HMBC correlations of 1 8.Published as part of Pei, Yue-Hu, Zhang, Li-Hua, Wu, Xi-Le,...
Fig. 7. The Mo2(OAc)4 induced circular dichroism (ICD) spectrum of compound 3a in anhydrous DMSO wit...
Fig. 1. Chemical structures of compounds 1–11.Published as part of Pei, Yue-Hu, Zhang, Li-Hua, Wu, X...
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).P...
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.Published as part of Yan, Wei, Ji, Wenxia, Ping, ...