Chemical Examination of the Roots of Cissampelospareira Linn.: Part III - Structure & Stereochemistry of Hayatinin
IR@CDRI: CSIR-Central Drug Research Institute, Lucknow
View Archive InfoField | Value | |
Creator |
Tihatnagar, A K
Popli, S P |
|
Date |
2010-08-23T10:25:46Z
2010-08-23T10:25:46Z 1967 |
|
Identifier |
Indian Journal of Chemistry,1967,5,102
http://hdl.handle.net/123456789/559 |
|
Description |
Sodium and liquid ammonia reduction of hayatinin ethyl ether affords a non-phenolic component,
identified as dl-4'-O-methyl-7-0-ethyl-N-methylcoclaurine, and a phenolic component
identified as dl-N-methylcoclaurine. The structures of these two fragments have been confirmed
by nuclear magnetic resonance and mass spectral data as well as the synthesis of the
former by usual methods. This establishes the structure of hayatinin as 4"-O-methyl-bebeerine
proposed earlier by Bhattacharji et al. [J. scient. indo Res., 21B (1962), 428]. The optical inactivity
of hayatinin as well as of phenolic and non-phenolic fragments suggests that hayatinin isolated
from this plant is a racemic mixture.
|
|
Format |
2112984 bytes
application/pdf |
|
Language |
en
|
|
Subject |
Cissampelospareira
Hayatinin Menispermaceae Cycleanine, |
|
Title |
Chemical Examination of the Roots of Cissampelospareira Linn.: Part III - Structure & Stereochemistry of Hayatinin
|
|
Type |
Article
|
|