Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Addendum Venenatine

Govindachari et al. have recently recorded the extraction of reserpine, venenatine (LXXVII), and 3-isovenenatine from the bark of Alstonia venenata R. Br. (98). 3-Isovenenatine may be identical with alstovenine, isolated earlier from the same species by Ray and Chatterjee (99), together with a second, unnamed base, m.p. 192°. [Pg.202]

Research Department, CIBA Pharmaceutical Company, Division oj CIBA Corporation, Summit, New Jersey [Pg.203]

The alkaloids can be conveniently grouped as shown in Table I, and it should be noted that the trivial names currently used obscure their similarities. [Pg.203]

Many of the alkaloids suffer facile autoxidation to yield hydroperoxy-and hydroxyindolenines, whose further degradation products are 4-hydroxyquinolines and pseudoindoxyls (Table I). Therefore, the [Pg.203]

Oxidation and rearrangement products of parent bases C. Acetyl side chain R3 = 0 [Pg.205]


See other pages where Addendum Venenatine is mentioned: [Pg.202]    [Pg.202]   


SEARCH



Addenda

Venenatine

© 2024 chempedia.info