Journal of the Chemical Society, Part 4, Pages 3513-4668The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 4089
... Chem . Soc . , 1953 , 75 , 4484 . 3 Johnson and Kay , J. , 1961 , 2418 . 4 Dean and Girdler , Chem . and Ind . , 1960 , 100 . 5 Caughey and Corwin , J. Amer . Chem . Soc . , 1955 , 77 , 1509 . • Rothemund and Menotti , J. Amer . Chem ...
... Chem . Soc . , 1953 , 75 , 4484 . 3 Johnson and Kay , J. , 1961 , 2418 . 4 Dean and Girdler , Chem . and Ind . , 1960 , 100 . 5 Caughey and Corwin , J. Amer . Chem . Soc . , 1955 , 77 , 1509 . • Rothemund and Menotti , J. Amer . Chem ...
Page 4411
... Chem . , 1948 , 20 , 1150 . ( a ) Oster and Oster , J. Pharmacol . , 1945 , 85 , 332 ; ( b ) Abrahamson , J. Biol . Chem . , 1949 , 178 , 179 ; ( c ) Wilbur , Bernheim , and Shapiro , Arch . Biochem . , 1949 , 24 , 305 ; ( d ) Donnan ...
... Chem . , 1948 , 20 , 1150 . ( a ) Oster and Oster , J. Pharmacol . , 1945 , 85 , 332 ; ( b ) Abrahamson , J. Biol . Chem . , 1949 , 178 , 179 ; ( c ) Wilbur , Bernheim , and Shapiro , Arch . Biochem . , 1949 , 24 , 305 ; ( d ) Donnan ...
Page 4442
... Chem . Soc . , 1960 , 82 , 5135 , 5141 . Beringer , Brierley , Drexler , Gindler , and Lumpkin , J. Amer . Chem . Soc . , 1953 , 75 , 2708 . 5 Beringer and Gindler , J. Amer . Chem . Soc . , 1955 , 77 , 3203 . ( a ) Beringer , Forgione ...
... Chem . Soc . , 1960 , 82 , 5135 , 5141 . Beringer , Brierley , Drexler , Gindler , and Lumpkin , J. Amer . Chem . Soc . , 1953 , 75 , 2708 . 5 Beringer and Gindler , J. Amer . Chem . Soc . , 1955 , 77 , 3203 . ( a ) Beringer , Forgione ...
Contents
4028 | 3507 |
Nucleophilic reactivity | 3513 |
Molecular polarisability Dipole moments molar Kerr constants and apparent | 3523 |
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absorption acetic acid acetic anhydride acetone acetoxylation acetyl added alcohol alkaline alumina aluminium Amer amine atoms band benzene benzyl bond bromide Calc carbon carbonyl chabazite Chem chloride chloroform chromatography cm.¹ compounds concentration crystals decomp diethyl diluted dimethylformamide diol dissolved distilled dried ester ethanol ethyl acetate evaporated EXPERIMENTAL extracted with ether filtrate formation Found fraction gave give heated hydrochloric acid hydrochloride hydrogen hydrolysis hydroxyl infrared iodide isomers K₁ ketone light petroleum lithium lithium aluminium hydride log ɛ m. p. and mixed mixed m. p. mixture mole molecules needles nitrate nitric acid nitrogen o-xylene obtained optical oxide oxygen petroleum b. p. phenol picrate potassium precipitated prepared proton pyridine rate constants reaction recrystallised refluxed requires residue room temperature salt sodium hydroxide solvent spectra spectrum stirred structure substitution sulphuric acid Table values washed yield