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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Page 5771
Chemical Society (Great Britain). DIVISION OF THE JOURNAL OF THE CHEMICAL SOCIETY THE Council of The Chemical Society , believing that the size of the Journal is reducing its acceptability as a medium for publication of original research ...
Chemical Society (Great Britain). DIVISION OF THE JOURNAL OF THE CHEMICAL SOCIETY THE Council of The Chemical Society , believing that the size of the Journal is reducing its acceptability as a medium for publication of original research ...
Page 5773
Chemical Society (Great Britain). DIVISION OF THE JOURNAL OF THE CHEMICAL SOCIETY THE Council of The Chemical Society , believing that the size of the Journal is reducing its acceptability as a medium for publication of original research ...
Chemical Society (Great Britain). DIVISION OF THE JOURNAL OF THE CHEMICAL SOCIETY THE Council of The Chemical Society , believing that the size of the Journal is reducing its acceptability as a medium for publication of original research ...
Page 6708
... chemical shifts at lower field than the < -protons because of ( a ) the effect of the conjugated carbonyl group , and ( b ) the aromatic ring current . When the relative chemical shifts for the a- and ẞ - protons for the substituted ...
... chemical shifts at lower field than the < -protons because of ( a ) the effect of the conjugated carbonyl group , and ( b ) the aromatic ring current . When the relative chemical shifts for the a- and ẞ - protons for the substituted ...
Contents
6613 | 5783 |
Transitionmetal quinoxaline complexes Part II Copper1 derivatives | 5784 |
ptolyl | 5785 |
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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 CH₂ Chem chloride chloroform chromatography cm.¹ colourless complex compounds concentration crystallised decomp derivatives dibromide dilute dissolved distilled elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate fluoride Found fraction gave give heated under reflux hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum 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 protons pyridine Raney nickel reaction requires residue ring room temperature salt showed sodium sodium hydroxide solid solution solvent spectra structure sulphide sulphoxide sulphuric Table thionyl chloride vacuo values VIII yellow yield