2013
DOI: 10.1016/j.bse.2012.09.024
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Alkaloids from the leaves of Monodora crispata Engl. and Diels and M. brevipes Benth. (Annonaceae)

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Cited by 6 publications
(13 citation statements)
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“…296.1281 mDa =0.1). The NMR spectra of 2 (Table 2) exhibited characteristic signals at δH 2.56 ppm (3H, s) and δC 42.7ppm, corresponding to an aporphine alkaloid, suchlike an N-methyl (Kablan et al, 2013;Dade et al, 2017). The combined analysis of its 13 C NMR and HSQC spectra revealed the presence of eighteen carbons: five methine, four methylene and eight quaternary carbon atoms.…”
Section: Resultsmentioning
confidence: 99%
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“…296.1281 mDa =0.1). The NMR spectra of 2 (Table 2) exhibited characteristic signals at δH 2.56 ppm (3H, s) and δC 42.7ppm, corresponding to an aporphine alkaloid, suchlike an N-methyl (Kablan et al, 2013;Dade et al, 2017). The combined analysis of its 13 C NMR and HSQC spectra revealed the presence of eighteen carbons: five methine, four methylene and eight quaternary carbon atoms.…”
Section: Resultsmentioning
confidence: 99%
“…1) were established according to their spectral data (NMR, IR and MS). Their stereochemistry was proposed on the basis of optical rotation measurement, in comparison with the literature (Hocquemiller et al, 1981;Spiff et al, 1984;Chang et al, 1995;Slvaki al., 1996;Kablan et al, 2013, Dade et al, 2017. [(1H, dd (8.4, 1.6), H-6)] and 8.18 (1H, H-4).…”
Section: Isolationmentioning
confidence: 99%
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“…Eleven aporphines alkaloids ( Figure 1 (11) isolated from the dried powdered leaves of M. crispata and brevipes [11,12] were used in this study. …”
Section: Isolated Compoundsmentioning
confidence: 99%