Journal of the Chemical SocietyThe Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 512
... reactions in which the lead - carbon bond is cleaved before the lead - lead bond . Reaction of the alkyl compounds with ethanolic hydrogen chloride was incomplete in the five - minute reaction period , but in chloroform hexamethyl ...
... reactions in which the lead - carbon bond is cleaved before the lead - lead bond . Reaction of the alkyl compounds with ethanolic hydrogen chloride was incomplete in the five - minute reaction period , but in chloroform hexamethyl ...
Page 532
... reaction represents the isomeric rearrange- ment of 1 - phenylallyl chloride to cinnamyl chloride ; the second concerns the reaction of the latter with triethylamine . First - order rate constants calculated from the second part ...
... reaction represents the isomeric rearrange- ment of 1 - phenylallyl chloride to cinnamyl chloride ; the second concerns the reaction of the latter with triethylamine . First - order rate constants calculated from the second part ...
Page 1108
... reactions which may be encountered are reduction , nuclear coupling , and participation of solvent in a substitution reaction . AROMATIC substitutions of type ( 1 ) , which are effected homogeneously in organic solvents between aryl ...
... reactions which may be encountered are reduction , nuclear coupling , and participation of solvent in a substitution reaction . AROMATIC substitutions of type ( 1 ) , which are effected homogeneously in organic solvents between aryl ...
Contents
NO PAGE | 1 |
Nucleophilic reactivity Part IV Competing bimolecular substitution | 5 |
The biosynthesis of fungal metabolites Part I Two different pathways | 16 |
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absorption acetic acid acetic anhydride alkaline aluminium chloride Amer amine ammonia anhydride aqueous aromatic atoms band benzene bond bromide Calc carbon Chem chloride chloroform chromatography complex compound concentration coupling constants crystallised crystals decomp decomposition derivative dilute dimethyl dimethyl ether dioxan distilled dried Elution equation erythroaphin-fb erythroaphins ester ethanol ether ethyl ethyl acetate evaporated EXPERIMENTAL extracted formation Found fraction gave halides hydrochloric acid hydrogen hydrolysis infrared infrared spectra iodide irradiated isomer k₂ ligand light petroleum m. p. and mixed maltose manganese(III method mixed m. p. mixture mole molecule mµ log nitrogen obtained oxidation oxygen phenyl piperidine potassium precipitate prepared protoaphin proton pyridine quinone reaction recrystallised reflux requires residue room temperature salt sample sodium hydroxide solution solvent spectrum structure substitution Table ultraviolet values Vmax washed yellow yield