Quarterly Journal of the Chemical Society of London, Pages 3324-4156 |
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Page 2997
... glucose and fructose in the presence of maltose , sucrose , glucose 1 - phosphate , and streptomycin A sulphate ( Table 3 ) . The total reducing sugars in the monosaccharide fraction were determined by Shaffer and Hartmann's method . 15 ...
... glucose and fructose in the presence of maltose , sucrose , glucose 1 - phosphate , and streptomycin A sulphate ( Table 3 ) . The total reducing sugars in the monosaccharide fraction were determined by Shaffer and Hartmann's method . 15 ...
Page 3022
... glucose , with the properties recorded by these authors , but each compound required additional purification on either powdered cellulose or carbon - Celite columns to remove traces of glucose . Repeated recrystallisation from absolute ...
... glucose , with the properties recorded by these authors , but each compound required additional purification on either powdered cellulose or carbon - Celite columns to remove traces of glucose . Repeated recrystallisation from absolute ...
Page 3392
... glucose was eluted with a 2 % sodium carbonate solution ( 180 ml . ) , and sodium ions were removed from the eluate ... glucose , but no acidic or neutral degradation products , was established . De - Acidite G ( −16 + 50 mesh ) . A ...
... glucose was eluted with a 2 % sodium carbonate solution ( 180 ml . ) , and sodium ions were removed from the eluate ... glucose , but no acidic or neutral degradation products , was established . De - Acidite G ( −16 + 50 mesh ) . A ...
Contents
ii | 2842 |
Catalytic hydrogenation | 2845 |
Garden J F and Thomson R H | 2851 |
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Common terms and phrases
4-triazine absorption acetic acid acetic anhydride acetone acidified added alcohol alkali alkyl Amer amine aqueous sodium atom band benzene benzyl boiling bromine Calc carbonate carbonyl Chem chloroform chromatography CO₂H colourless compound concentration containing cooled crystallised cyclisation decomp derivative diethyl dilute dioxan dioxide diphenyl dissolved distilled dried eluted ester ethanol ethyl acetate evaporated filtered filtrate fluorene formation formed Found fraction gave give H₂O heated hydrochloric acid hydrogen chloride hydrolysis infrared iodide isatin isolated ketone lactone light petroleum b. p. lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mole needles nitric acid nitrogen obtained oxidation perchloric phenyl potassium hydroxide precipitate prepared prisms pyridine reaction reagent reduced refluxed requires residue room temperature salt separated sodium hydroxide solid solution solvent spectra structure sulphuric acid Table titration washed yellow yield