1997
DOI: 10.1590/s0100-40421997000500002
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Atribuição inequívoca de deslocamentos químicos de RMN de ¹H e 13C de plumierídeo isolado da Allamanda cathartica

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Cited by 7 publications
(7 citation statements)
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“…The purity of the compound was assessed by high performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) analysis, through comparison with the literature and direct comparison with original samples. 13,21,35 Plumieride presented a purity > 98%. Methanol and acetonitrile were purchased from Tedia® (HPLC grade).…”
Section: Chemicalsmentioning
confidence: 93%
See 1 more Smart Citation
“…The purity of the compound was assessed by high performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) analysis, through comparison with the literature and direct comparison with original samples. 13,21,35 Plumieride presented a purity > 98%. Methanol and acetonitrile were purchased from Tedia® (HPLC grade).…”
Section: Chemicalsmentioning
confidence: 93%
“…The compound was analyzed by HPLC and NMR, then the data were compared with those found in the literature or with data of the standard previously isolated. 13,21,35 …”
Section: Extraction and Isolation Of Plumieridementioning
confidence: 99%
“…All the compounds were identified based on their spectral data, by comparison with the literature (Malheiros et al 1997, Schmidt et al, 2006 and direct comparison with original samples.…”
Section: Isolation and Identification Of Componentsmentioning
confidence: 99%
“…From this procedure a mixture of -sitosterol and stigmasterol, plumericin, plumieride, ursolic acid, 3-O--glucopyranosylsitosterol and a mixture of sugars were obtained. The compounds were analyzed by nuclear magnetic resonance (NMR) and their chemical shifts were compared with those found in the literature or with data of the standards previously isolated (Ganapaty et al, 1988, Abdel-Kader et al, 1997, Malheiros et al, 1997, Schmidt et al, 2006.…”
Section: Identification Of Active Compounds In Dcm Fractionmentioning
confidence: 99%
“…The product HA1 was visualized under visible and UV light (254 nm) and submitted to nuclear magnetic resonance ( 1 H NMR and 13 C NMR) analyses. The chemical structure of isolated compound was identified by nuclear magnetic resonance (Bruker 400) using 1 H NMR (400 MHz), 13 C NMR (100 MHz), 2D NMR analysis, and by comparison of spectral data with those available in the literature (Malheiros et al, 1997). MeOD was used as solvent for HA1.…”
Section: Isolation and Structure Elucidation Of Ha1mentioning
confidence: 99%