Journal of the Chemical SocietyThe Society., 1958 |
From inside the book
Results 1-3 of 80
Page 2870
... Amer . Chem . Soc . , 1956 , 78 , 3710 . 24 Challenger and Greenwood , J. , 1950 , 26 . 25 Schönberg , Ber . , 1935 , 68 , 163 . 26 Jacobsen , Harvey , and Jensen , J. Amer . Chem . Soc . , 1955 , 77 , 6064 . 27 Lien , McCaulay , and ...
... Amer . Chem . Soc . , 1956 , 78 , 3710 . 24 Challenger and Greenwood , J. , 1950 , 26 . 25 Schönberg , Ber . , 1935 , 68 , 163 . 26 Jacobsen , Harvey , and Jensen , J. Amer . Chem . Soc . , 1955 , 77 , 6064 . 27 Lien , McCaulay , and ...
Page 2973
... Amer . Chem . Soc . , 1957 , 79 , 6407 . † Presented in part at the Amer . Chem . Soc . Meeting , Miami , 1957 , Abstracts , p . 7C . In other papers of this series , Ring Index names ( pyrazolo [ 3 : 4 - d ] pyrimidine and pyrazolo ...
... Amer . Chem . Soc . , 1957 , 79 , 6407 . † Presented in part at the Amer . Chem . Soc . Meeting , Miami , 1957 , Abstracts , p . 7C . In other papers of this series , Ring Index names ( pyrazolo [ 3 : 4 - d ] pyrimidine and pyrazolo ...
Page 3440
... Amer . , 1954 , 43 , 941 ) in order to justify an accuracy of ± 1 cm . - 1 . • Insufficient available for accurate ... Amer . Chem . Soc . , 1927 , 49 , 810. Clemo and Howe , J. , 1955 , 3552. Matsumura , J. Amer . Chem . Soc . , 1930 ...
... Amer . , 1954 , 43 , 941 ) in order to justify an accuracy of ± 1 cm . - 1 . • Insufficient available for accurate ... Amer . Chem . Soc . , 1927 , 49 , 810. Clemo and Howe , J. , 1955 , 3552. Matsumura , J. Amer . Chem . Soc . , 1930 ...
Contents
Chemical applications of nuclear quadrupole resonance spectroscopy Part | 2634 |
541 | 2637 |
the isomerisation of normal to isosapogenins | 2645 |
114 other sections not shown
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Common terms and phrases
absorption acetic acid acetic anhydride acetone acetylene activation energy added alkaline alkyl allogibberic alumina Amer amine atom benzene boiling bond bromine Calc carbon cation CH₂ Chem chloride chloroform chromatographed colourless compound concentrated containing cooled crystallised from ethanol crystals curves cyclic sulphide cyclohexene decomp derivative dilute dimethylformamide diphenylene dissolved distilled disulphide dried eluted ester ethanol ether evaporated extracted filtered filtrate formation Found fraction gave give heated hydrochloric acid hydrogen pressure hydrogen sulphide hydrogenolysis hydrolysis infrared spectrum iodide iodine ketone light petroleum b. p. lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mole molecule needles nitric acid nitrogen obtained olefin oxide picrate polysulphide potassium hydroxide precipitated prepared prisms pyridine reaction reduction reflux requires residue room temperature saturated sodium hydroxide solid solvent spectra substituent sulphuric acid synthesis thiol ultraviolet vacuo washed yellow yield