Strychnos 1990 - 2004 - Crops for the Future

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Author Title Year Source title Reference Abstract Saxton, J. E. Recent progress in the chemistry of the monoterpenoid indole alkaloids 1995 Natural Product Reports 12(4): 385-411 - Author Title Year Source title Reference Zong, Y. Y. and C. T. Che Determination of strychnine and brucine by capillary zone electrophoresis 1995 Planta Medica 61(5): 456-458 Abstract A procedure for quantitative estimation of strychnine and brucine in the extracts of Strychnos nuxvomica seeds by capillary zone electrophoresis (CZE) was developed. The buffer solution used was 10mM phosphate buffer-MeOH (9:1), pH 2.5. The linear calibration range was 0.01-0.15 mg/ml. This method is useful for the qualitative and quantitative determination of strychnine and brucine in p lant drug samples, as well I as in human plasma. Author Title Year Source title Reference Adinolfi, M., M. M. Corsaro, R. Lanzetta, M. Parrilli, G. Folkard, W. Grant and J. Composition of the coagulant polysaccharide fraction from Strychnos potatorum s 1994 Carbohydrate Research 263(1): 103-110 Abstract The composition of the coagulant polysaccharide fraction from Strychnos potatorum seeds is described. This fraction comprises a 1:1.7 mixture of a galactomannan and a galactan. The structure of these polysaccharides is also discussed. In addition, the coagulant properties of the polysaccharide fractions of two other Strychnos species, innocua and nux-vomica, have been assayed.
Author Title Year Source title Reference Abstract Amat M; Sathyanarayana S; Hadida S; Bosch J Short formal syntheses of indole alkaloids of the uleine and Strychnos groups 1994 Tetrahedron Letters 35(38): 7123 - Author Title Year Source title Reference Abstract Cai, B. C., H. Wu, X. W. Yang and M. Hattori Analysis of spectral data for ^1^3cnmr of sixteen Strychnos alkaloids 1994 Acta Pharmaceutica Sinica 29(1): 48 - Author Title Year Source title Reference Catena J; Valls N; Bosch J; Bonjoch J The pummerer cyclization route to the ibophyllidine alkaloids - total synthesis of ( 1994 Tetrahedron Letters 35(25): 4433-4436 Abstract Pummerer cyclization of beta-aminoethyl sulfoxide 6 was effectively achieved using TFAA-TFA in toluene at 80 degrees C. The cyclized product 7 was then converted to the alkaloid deethylibophyllidine. The required pyrrolo[3,2-c]carbazole 6 was prepared in five steps from 4- m e t h o x y p h e n e t h y l a m i n e .
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