Fig. 2. (a) HMBC and 1H– 1H COSY (b) NOESY correlations of compound 1.Published as part of Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Liang, Zhang, Jie-Yao, Li, Ya & Gao, Kun, 2020, Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata, pp. 1-12 in Phytochemistry (112230) 171 on page 6, DOI: 10.1016/j.phytochem.2019.112230, http://zenodo.org/record/829389
Fig. 2. Selected HMBC and 1H– 1H COSY correlations of compounds 1–4, 6, 8, 12, and 16.Published as p...
Fig. 2. Key NOESY correlations of compounds 4, 9, 11, 14 (R ¼ (CH2)14CH3, in green), 18 and 19. (For...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...
Fig. 4. (a) HMBC and 1H–1H COSY (b) NOESY correlations of compound 25.Published as part of Li, Hang-...
Fig. 1. Structures of compounds 1–34.Published as part of Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Liang...
Fig. 3. ORTEP drawing of 1, 3, and 27.Published as part of Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Lian...
Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Liang, Zhang, Jie-Yao, Li, Ya, Gao, Kun (2020): Phytotoxic neo-...
Fig. 5. Phytotoxic effects of the MeOH extract, the EtOAc fraction, and the n-BuOH fraction on the g...
Fig. 6. Phytotoxic effects of compound 2, 3, 15, 18, 20, 25, 29, 32, and glyphosate (positive contro...
Fig. 7. Phytotoxic effects of compound 2, 20, 21, 22, 25, 27, and glyphosate (positive control) on t...
Fig. 2. 1 H– 1 H COSY and key HMBC (H→C) correlations of compounds 1, 5 and 9.Published as part of M...
Fig. 3. The main chemical skeletons of clerodane diterpenoids from Scutellaria spp.Published as part...
Fig. 2. The structure and numbering system of clerodane skeleton.Published as part of Maleki, Sina, ...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4, 5 and 9.Published as part of Munissi, Joan J.E....
Fig. 2. (a) Selected COSY and HMBC correlations of 1 (b) Selected NOESY correlations of 1 (c) Select...
Fig. 2. Selected HMBC and 1H– 1H COSY correlations of compounds 1–4, 6, 8, 12, and 16.Published as p...
Fig. 2. Key NOESY correlations of compounds 4, 9, 11, 14 (R ¼ (CH2)14CH3, in green), 18 and 19. (For...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...
Fig. 4. (a) HMBC and 1H–1H COSY (b) NOESY correlations of compound 25.Published as part of Li, Hang-...
Fig. 1. Structures of compounds 1–34.Published as part of Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Liang...
Fig. 3. ORTEP drawing of 1, 3, and 27.Published as part of Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Lian...
Li, Hang-Ying, Wei, Wen-Jun, Ma, Kai-Liang, Zhang, Jie-Yao, Li, Ya, Gao, Kun (2020): Phytotoxic neo-...
Fig. 5. Phytotoxic effects of the MeOH extract, the EtOAc fraction, and the n-BuOH fraction on the g...
Fig. 6. Phytotoxic effects of compound 2, 3, 15, 18, 20, 25, 29, 32, and glyphosate (positive contro...
Fig. 7. Phytotoxic effects of compound 2, 20, 21, 22, 25, 27, and glyphosate (positive control) on t...
Fig. 2. 1 H– 1 H COSY and key HMBC (H→C) correlations of compounds 1, 5 and 9.Published as part of M...
Fig. 3. The main chemical skeletons of clerodane diterpenoids from Scutellaria spp.Published as part...
Fig. 2. The structure and numbering system of clerodane skeleton.Published as part of Maleki, Sina, ...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4, 5 and 9.Published as part of Munissi, Joan J.E....
Fig. 2. (a) Selected COSY and HMBC correlations of 1 (b) Selected NOESY correlations of 1 (c) Select...
Fig. 2. Selected HMBC and 1H– 1H COSY correlations of compounds 1–4, 6, 8, 12, and 16.Published as p...
Fig. 2. Key NOESY correlations of compounds 4, 9, 11, 14 (R ¼ (CH2)14CH3, in green), 18 and 19. (For...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...