Journal of the Chemical Society, Part 5The Society., 1965 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 69
Page 5952
... Methyl - substituted Amines . - 4 - Methyl - 2 - naphthylamine and 4 - methyl - 2 - dimethyl- aminonaphthalene are stronger bases than the parent amines by 0.11 and 0.21 pK unit , respectively . The effect of the 4 - methyl substituent ...
... Methyl - substituted Amines . - 4 - Methyl - 2 - naphthylamine and 4 - methyl - 2 - dimethyl- aminonaphthalene are stronger bases than the parent amines by 0.11 and 0.21 pK unit , respectively . The effect of the 4 - methyl substituent ...
Page 6225
... methyl ester , prepared with methanol and hydrogen chloride , formed plates in methanol , m . p . 146 ° ( Found : C ... Methyl M. P. Found ( % ) H N S Required ( % ) Formula C H N S picrate ( orange - red needles ) 5 - Methyl picrate ...
... methyl ester , prepared with methanol and hydrogen chloride , formed plates in methanol , m . p . 146 ° ( Found : C ... Methyl M. P. Found ( % ) H N S Required ( % ) Formula C H N S picrate ( orange - red needles ) 5 - Methyl picrate ...
Page 6453
... methyl steroids are given in the Table . The results support the configurations assigned at C - 3 to the epimers ( VIII and X ; R = H ) ; thus , the three - proton singlet for the 5ẞ - methyl group in ( X ; R = H ) occurs at lower field ...
... methyl steroids are given in the Table . The results support the configurations assigned at C - 3 to the epimers ( VIII and X ; R = H ) ; thus , the three - proton singlet for the 5ẞ - methyl group in ( X ; R = H ) occurs at lower field ...
Contents
ptolyl | 5785 |
The crystal structure of dipotassium bistrimethylenedinitramine nickelate11 | 5801 |
Coordination compounds having carboxylic esters as ligands | 5826 |
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absorption acetic acid acetic anhydride acetone Amer amine anhydride aqueous atoms band benzene benzyl bond borazocine boron bromide Calc carbon carbon tetrachloride carbonyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration constants crystallised decomp derivatives dilute dissolved distilled eluted ester ethanol ether ethyl acetate evaporated extracted filtered filtrate fluoride Found fraction gave give H₂O heated under reflux hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum iodide isolated isomer ketone ligand light petroleum m. p. and mixed methyl mixed m. p. mixture mmoles mole molecule n.m.r. spectrum nitrogen obtained olefin optical oxazolone oxide peak perchlorate phenyl potassium prepared proton pyridine reaction requires residue ring room temperature salt showed sodium sodium hydroxide solid soluble solution solvent spectra structure sulphide sulphoxide sulphuric Table thionyl chloride vacuo values VIII yellow yield