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415 results for “diterpenoid”
Fig. 9 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 9. Experimental ECD spectra of 5 and 6 in MeCN.
Fig. 7. Proposed biosynthetic relationships between compounds 7 and 1–3 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 7. Proposed biosynthetic relationships between compounds 7 and 1–3.
Fig. 4 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 4. ORTEP drawing of 1.
Fig. 5 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 5. Experimental and calculated ECD spectra of 2 in MeCN.
Fig. 2. 1H–1H in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 2. 1H–1H COSY (for 2–4, and 6) and selected HMBC correlations (for 1–6).
Fig. 3 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 3. Key NOE correlations of 1–6.
Fig. 1 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 1. Chemical structures of 1–21.
Fig. 8 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 8. Experimental and calculated ECD spectra of 4 in MeCN.
Fig. 6 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 6. Experimental and calculated ECD spectra of 3 in MeCN.
Fig. 5 in Ent-abietane diterpenoid lactone glycosides and a phenolic glycoside from Phlogacanthus pulcherrimus T. Anderson with cytotoxic and cancer chemopreventive activities
Fig. 5. Experimental and calculated ECD spectra of compounds 1, 2, 5, 7, 8, and 9.
Fig. 3 in Ent-abietane diterpenoid lactone glycosides and a phenolic glycoside from Phlogacanthus pulcherrimus T. Anderson with cytotoxic and cancer chemopreventive activities
Fig. 3. Key COSY (), HMBC (H C), and NOESY () correlations of compound 7.
Fig. 2 in Ent-abietane diterpenoid lactone glycosides and a phenolic glycoside from Phlogacanthus pulcherrimus T. Anderson with cytotoxic and cancer chemopreventive activities
Fig. 2. Key COSY (), HMBC (H C), and NOESY () correlations of compound 1.
Fig. 4 in Ent-abietane diterpenoid lactone glycosides and a phenolic glycoside from Phlogacanthus pulcherrimus T. Anderson with cytotoxic and cancer chemopreventive activities
Fig. 4. Key HMBC (H C), and NOESY () correlations of compound 8.
Fig. 1 in Ent-abietane diterpenoid lactone glycosides and a phenolic glycoside from Phlogacanthus pulcherrimus T. Anderson with cytotoxic and cancer chemopreventive activities
Fig. 1. Structures of compounds 1–20.
Fig. 7 in Ent-abietane and ent-pimarane diterpenoids from Croton mubango (Euphorbiaceae)
Fig. 7. (a) 1H–1H COSY and key HMBC (H→C) correlations of 14; (b) Key NOESY correlations of 14.
Fig. 1 in Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone
Fig. 1. Structures of compounds 1–6.
Fig. 4 in Ent-abietane and ent-pimarane diterpenoids from Croton mubango (Euphorbiaceae)
Fig. 4. (a) 1H–1H COSY and key HMBC (H→C) correlations of 4; (b) Key NOESY correlations of 4.
Fig. 8 in Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone
Fig. 8. Possible resonance structures of unpaired electrons in the triplet state of 6.
Fig. 1 in Ent-abietane and ent-pimarane diterpenoids from Croton mubango (Euphorbiaceae)
Fig. 1. Structures of ent-diterpenoids 1–14 isolated from Croton mubango.
Fig. 3 in Ent-abietane and ent-pimarane diterpenoids from Croton mubango (Euphorbiaceae)
Fig. 3. (a) 1H–1H COSY and key HMBC (H→C) correlations of 2; (b) Key NOESY correlations of 2.
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OpenNeuro
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