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Chemical Examination of the Roots of Cissampelospareira Linn.: Part III - Structure & Stereochemistry of Hayatinin

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field 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