(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This alkaloid from the leaf extract of Voacanga africana has the above structure in neutral or basic media as determined by spectral data, particularly the mass spectra. In acid solution it exists as the quaternary base. Reduction with KBH4 yields Voaphylline (q.v.) and conversely the base may be formed from the latter by oxidation with peracetic acid.

Einzelnachweise

Kunesch, Das, Poisson., Bull. Soc. Chim. Fr., 3551 (1967)

(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• (1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol
• Voaphylline hydroxyindolenine
• Voaphylline hydroxyindolenine【neutral】
• 2H-3,13-Methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol, 13-ethyl-4,5,11,12,13,13a-hexahydro-, (1aR,5aR,13S,13aS)-
• 18269-16-4