1972
DOI: 10.1016/s0040-4039(01)84388-4
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Euphorbetin: a new bicoumarin from L.

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1977
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Cited by 22 publications
(8 citation statements)
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“…The overall isolation yield was about 0.25−0.30 g/kg of seeds. An unexpected asset of the KCN method is that precipitation of L 1 ( 2 ) takes place during the transesterification of the ingenol-based L-factors, allowing the recovery of the major L-factor by simple filtration (Scheme ) . A certain selectivity in the hydrolysis step could also be achieved with Zemplén methanolysis under carefully controlled conditions (see Experimental Section).…”
Section: Resultsmentioning
confidence: 99%
“…The overall isolation yield was about 0.25−0.30 g/kg of seeds. An unexpected asset of the KCN method is that precipitation of L 1 ( 2 ) takes place during the transesterification of the ingenol-based L-factors, allowing the recovery of the major L-factor by simple filtration (Scheme ) . A certain selectivity in the hydrolysis step could also be achieved with Zemplén methanolysis under carefully controlled conditions (see Experimental Section).…”
Section: Resultsmentioning
confidence: 99%
“…Peaks 42 and 43 were identified as umbelliferone and scopoletin by spiking experiments with authentic standards. Peak 2 with a pseudomolecular ion at m / z 353.02919 was identified as the dicoumarin euphorbetin ( Figure S1b ) [ 29 ].…”
Section: Resultsmentioning
confidence: 99%
“…Using co-elution procedures with already identified samples, we were able to identify peaks 10 and 13 as umbelliferone and scopoletin (3). Subject to further confirmation, peak 12 was identified as the dicoumarin euphorbetin because of its parent deprotonated ion at m/z 353.02919 [35,36]…”
Section: Coumarinsmentioning
confidence: 99%