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 67
Page 1223
... mixed m . p . 41-42 ° , and N - methylbenzamide ( 1 · 17 g . ) , m . p . and mixed m . p . 75—76 ° . Reactions of t - Butyl Methyl Sulphide .-- ( a ) With t - butyl peroxide at 140 ° . Reactions were carried out as before with the ...
... mixed m . p . 41-42 ° , and N - methylbenzamide ( 1 · 17 g . ) , m . p . and mixed m . p . 75—76 ° . Reactions of t - Butyl Methyl Sulphide .-- ( a ) With t - butyl peroxide at 140 ° . Reactions were carried out as before with the ...
Page 1765
... mixed m . p . 146–148 ° ( lit. , 6 m . p . 148 ° ) . Reduction of 6 - Chloro - 1 - methyl - 4 - cinnolone . — The cinnolone ( 0.5 g .; m . p . 160–162 ° ) and triethylamine ( 1 c.c. ) , in ethanol ( 50 c.c. ) , were hydrogenated with 10 ...
... mixed m . p . 146–148 ° ( lit. , 6 m . p . 148 ° ) . Reduction of 6 - Chloro - 1 - methyl - 4 - cinnolone . — The cinnolone ( 0.5 g .; m . p . 160–162 ° ) and triethylamine ( 1 c.c. ) , in ethanol ( 50 c.c. ) , were hydrogenated with 10 ...
Page 1990
... ( mixed m . p . and infrared spectrum ) with a sample prepared as below , and on oxidation with 30 % hydrogen peroxide in acetic acid at 50 ° for 15.0 hr . , gave 1,2 - dihydro - 3 - hydroxy - 1 - methyl - 2 - oxoquinoxaline ( VII ; R ...
... ( mixed m . p . and infrared spectrum ) with a sample prepared as below , and on oxidation with 30 % hydrogen peroxide in acetic acid at 50 ° for 15.0 hr . , gave 1,2 - dihydro - 3 - hydroxy - 1 - methyl - 2 - oxoquinoxaline ( VII ; R ...
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Common terms and phrases
1-methylheptyl 1-phenylethyl bromide absorption acetic acid acetone acetonitrile adducts alcohol Amer amine anhydride aniline aqueous atom benzene bond Calc calculated carbon carboxyl Chem chloroform chromatography complex compounds concentration correlation crystallised cyclopropane derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether experimental extracted fluorine formation Found fraction gave H₂O halides hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis mixed m. p. mixture mmoles mole mole-¹ molecular molecules nitrogen nucleophilic o-complex obtained oleyl alcohol optical orbitals oxaloacetic acid oxidation oxygen peak phenols phosphate phosphine picryl potassium prepared proton pyridine rate coefficients rate constants reaction reflux requires residue rotation shown similar sodium solution solvent spectra structure substituted sulphide t-butyl methyl t-butyl peroxide Table tetracyanoethylene titration toluene-p-sulphonate values yield