(5α,12β,19α)-2,3-Didehydro-1-methylaspidospermidine-3-carboxylic acid methyl ester Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

A further alkaloid isolated from Vinca minor L., this base is possibly optically inactive, the specific rotation reported being [α]_D 00 ± 2° (c 1.0, EtOH). The ultraviolet spectrum in EtOH has a broad absorption maximum at 338 mil and an inflexion at 310 mil. The structure has been confirmed by the synthesis of the (±)-form.

Einzelnachweise

Kokry, Dubravkova, Sefecovic.,Experientia, 18,564 (1962)
Mokryetal., ibid, 19,311 (1963)
Zachystalova, Strouf, Trojanek., Chern. & Ind., 610 (1963)
Synthesis: Kutney et al., J. Amer. Chern. Soc., 90,3891 (1968)

(5α,12β,19α)-2,3-Didehydro-1-methylaspidospermidine-3-carboxylic acid methyl ester Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(5α,12β,19α)-2,3-Didehydro-1-methylaspidospermidine-3-carboxylic acid methyl ester Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• (5α,12β,19α)-2,3-Didehydro-1-methylaspidospermidine-3-carboxylic acid methyl ester
• Minovin
• Minovine
• 19074-77-2