1990
DOI: 10.1016/0031-9422(90)85240-g
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An indolinic cryptoalkaloid from Strychnos mattogrossensis

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1992
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Cited by 13 publications
(7 citation statements)
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“…8) We can pose the question of whetter compound 1 has a role as a precursor in the biosynthesis of strychnine, 9) since 1 seems to be originated just before the formation of the Wieland-Gumlich aldehyde ( Fig. 2), but without hydroxylation at positions 3 and 18.…”
Section: 7)mentioning
confidence: 99%
“…8) We can pose the question of whetter compound 1 has a role as a precursor in the biosynthesis of strychnine, 9) since 1 seems to be originated just before the formation of the Wieland-Gumlich aldehyde ( Fig. 2), but without hydroxylation at positions 3 and 18.…”
Section: 7)mentioning
confidence: 99%
“…The structure of 1 is the 3-hydroxy-enolate of the known alkaloid nordiidrofluorocurarine, previously isolated from S. amazonica and S. froessi. 8) We can pose the question of whetter compound 1 has a role as a precursor in the biosynthesis of strychnine, 9) since 1 seems to be originated just before the formation of the Wieland-Gumlich aldehyde (Fig. 2), but without hydroxylation at positions 3 and 18.…”
Section: Resultsmentioning
confidence: 99%
“…S. mattogrossensis is a South American species growing in the tropical forest of the Amazon. The root, stem bark and twigs of this plant have been investigated and it is known to contain alkaloids, such as mattogrossine, strychnobrasiline, 12-hydroxy-11-methoxystrychnobrasiline (Angenot et al, 1990), and more recently 12-hydroxy-10,11-dimethoxystrychnobrasiline (Belem-Pinheiro, Couceiro, Imbiriba da Rocha, Monte, & Villar, 2002).…”
mentioning
confidence: 99%