1978
DOI: 10.1002/jps.2600670348
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Alkaloids from Lupinus argenteus var. stenophyllus

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Cited by 23 publications
(6 citation statements)
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“…A portion of the 430-mg residue was also analyzed by gc/ms. This corroborated the classical isolation studies and also provided evidence for carbomethoxypedicularine (11). (+)-Boschniakine 9.-This was identified by optical rotation, uv, 'H-nmr (360 MHz), 13C-nmr, and mass spectra and by a comparison with a standard sample.…”
Section: Alkaloid Isolations and Analysessupporting
confidence: 80%
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“…A portion of the 430-mg residue was also analyzed by gc/ms. This corroborated the classical isolation studies and also provided evidence for carbomethoxypedicularine (11). (+)-Boschniakine 9.-This was identified by optical rotation, uv, 'H-nmr (360 MHz), 13C-nmr, and mass spectra and by a comparison with a standard sample.…”
Section: Alkaloid Isolations and Analysessupporting
confidence: 80%
“…int.) 262(1), 247(1), 223(100), 207(2), 124 (11), 112(22), 109(3), 58(54); NH3ci ms 265(100), 263(25), 249 (8), 223(25), 112 (5), 58 (20). These data correspond quite closely with those from tetrahydrorhombifoline (6,7) except that the 223 base peaks in the ei ms and the quasimolecular ion in the NH3 ci ms were exactly 16 mass units higher than in tetrahydrorhombifoline.…”
Section: Alkaloid Isolations and Analysesmentioning
confidence: 99%
See 1 more Smart Citation
“…results). The 5,6-dehydrolupanine (4) has been reported so far only from species which contain both lupanine (6) and -pyridone alkaloids (12,16,20). It is plausible to place this compound as the intermediate between lupanine (6) and anagyrine (8).…”
Section: Differentiated Plantsmentioning
confidence: 99%
“…Extraction and Isolation of Alkaloids. The dried, powdered (40 mesh) aboveground plant parts (200 g) were homogenized with MeOH and processed as usual (Keller and Zelenski, 1978) to give 1.30 g (0.65% of dry weight) of a crude alkaloid extract. TLC of this mixture over 0.25-mm layers of silica gel 60 GF 254 (Merck) with CHCl3-MeOH-18 M NH4OH (100:10:1) indicated the presence of three alkaloids located at R¡ 0.73,0.44, and 0.31 after spraying with Dragendorff reagent.…”
Section: Methodsmentioning
confidence: 99%