Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 43
Page 1408
... phosphate ( IV ; R = R ' = Me ) from uridine - 5 ' methyl hydrogen phosphate ( IV ; R = Me , R ' H ) using a 110 - molar excess of diazomethane , only traces of dimethyl ester being formed . In the same way , uridine - 2 ' , 3 ...
... phosphate ( IV ; R = R ' = Me ) from uridine - 5 ' methyl hydrogen phosphate ( IV ; R = Me , R ' H ) using a 110 - molar excess of diazomethane , only traces of dimethyl ester being formed . In the same way , uridine - 2 ' , 3 ...
Page 1411
... phosphate . Methylation of Uridine - 5 ′ Methyl Hydrogen Phosphate ( IV ; R Me , R ' H ) .- A solution of the pyridinium salt of uridine - 5 ′ methyl hydrogen phosphate ( 3.8 mg . ) in water ( 2 c.c. ) was shaken with ethereal ...
... phosphate . Methylation of Uridine - 5 ′ Methyl Hydrogen Phosphate ( IV ; R Me , R ' H ) .- A solution of the pyridinium salt of uridine - 5 ′ methyl hydrogen phosphate ( 3.8 mg . ) in water ( 2 c.c. ) was shaken with ethereal ...
Page 1931
... Phosphate . By A. LAPIDOT and DAVID SAMUEL . The kinetics of the hydrolysis of NN - diethylcarbamoyl phosphate have been studied in the range from pH 7 to 3.1N - perchloric acid . In basic solution it is hydrolysed very slowly at 100 ...
... Phosphate . By A. LAPIDOT and DAVID SAMUEL . The kinetics of the hydrolysis of NN - diethylcarbamoyl phosphate have been studied in the range from pH 7 to 3.1N - perchloric acid . In basic solution it is hydrolysed very slowly at 100 ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
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1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield