(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
One of the numerous alkaloids isolated from Vinca species, this base occurs in V. rosea L. and forms colourless crystals from MeOH. It is laevorotatory with[α]
26D - 58° (MeOH) and when crystallized from Me
2CO forms crystals containing solvent of crystallization, m.p. 181°C. The ultraviolet spectrum in MeOH has absorption maxima at 226, 282 and 290 mf.1. The alkaloid contains a primary alcoholic group and an imino group and yields the hemisulphate, m.p. 239- 241°C (dec.); the picrate, m.p. 226-8°C (dec.) and the O-acetate, m.p. 198°C;[α]
26D- 26° (MeOH).
Einzelnachweise
Svoboda et al., J. Pharm. Sci., 50,409 (1961)
Kutney, Brown., Tetrahedron Lett., 1815 (1963)
(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte