High resolution gas chromatography—Mass spectral analysis of carbohydrates using methoxyoxime acetates

1993 ◽  
Vol 4 (6) ◽  
pp. 256-260 ◽  
Author(s):  
Markus Herderich ◽  
Peter Schreier
1978 ◽  
Vol 31 (5) ◽  
pp. 1161 ◽  
Author(s):  
WJ Griffin

(�)-6β,7β-Dihydroxytropan-3α-yl benzoate was isolated in low yield (0.001%) from the roots of Erythroxylon australe. The aerial parts were found to contain meteloidine (0.014%), (�)-6β-hydroxytropan-3α-yl tiglate (0.001%), (+)-3α-hydroxynortropan-6β-yl tiglate (0.002%) and an unknown base (0.003%) which was tentatively identified as (+)-7- hydroxy-6-tigloyloxynortropan-3-yl 2-hydroxy-3-phenylpropionate. The configuration of the unknown base was not determined. Structures were indicated by N.M.R. and mass spectral analysis and the phenyl propionic acid moiety identified by gas chromatography.


Author(s):  
ALETI RAJAREDDY ◽  
SRINIVAS MURTHY M

Objective: The objective of this study was to synthesize and evaluate the anthelmintic activity (AA) of novel benzothiazole derivatives containing indole moieties (BDIM). Methods: The present works which involve the substituted isatin Schiff bases undergo acetylating and reacting with 2-aminobenzothiazole to give novel BDIM. Results: All the newly synthesized molecules (5a-5o) were characterized by Fourier-transform infrared spectroscopy, H_nuclear magnetic resonance, and mass spectral analysis along with physical data. The biological potentials of the newly synthesized compounds are evaluated for their AA using an Indian earthworm (Pheretima posthuma), and albendazole was used as standard drug. Conclusion: The synthesized compound 5f, 5n, and 5o showed good AA, whereas others exhibited significant activities.


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