(20S)-2,16-Didehydro-20-hydroxycuran-17-oic acid methyl ester Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

A further alkaloid from Vinca rosea L., forming colourless prisms when crystallized from MeOH. The ultraviolet spectrum has absorption maxima at 230, 293 and 328 mil. The base contains a tertiary hydroxyl group and an imino group and, with AC20 in pyridine, furnishes akuammicine (q.v.), by dehydration. Reduction with Zn dust in MeOH-H2S04 yields 2: 16-dihydroakuammicine after preparative thin-layer chromatography on silica gel.

Einzelnachweise

Svoboda et al., J. Pharm. Sci., 50, 409 (1961)
Structure:
Nakagawa et at., Chem. Ind., 1986 (1962)

(20S)-2,16-Didehydro-20-hydroxycuran-17-oic acid methyl ester Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(20S)-2,16-Didehydro-20-hydroxycuran-17-oic acid methyl ester Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
TargetMol Chemicals Inc.	+1-781-999-5354;	support@targetmol.com	United States	39037	58

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• (20S)-2,16-Didehydro-20-hydroxycuran-17-oic acid methyl ester
• Lochneridine
• Curan-17-oic acid, 2,16-didehydro-20-hydroxy-, methyl ester, (20α)- (9CI)
• 5980-01-8
• C20H24O3N2