Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 104
... reduction of 4 - t - butyl- cyclohexanone and dihydroisophorone has been studied at controlled potential and current density and it has been found that at relatively small cathodic potentials , in the presence of acetic acid , the ...
... reduction of 4 - t - butyl- cyclohexanone and dihydroisophorone has been studied at controlled potential and current density and it has been found that at relatively small cathodic potentials , in the presence of acetic acid , the ...
Page 380
... reduction of optically - active compounds afforded the inversion products , while Brown and Krishnamurthy suggested the possibility of a four- centre - type mechanism for the reduction of aryl halides . We report evidence that the reduction ...
... reduction of optically - active compounds afforded the inversion products , while Brown and Krishnamurthy suggested the possibility of a four- centre - type mechanism for the reduction of aryl halides . We report evidence that the reduction ...
Page 465
... reduction of organic halides to hydrocarbons is well known.1 The halogen may be chlorine , bromine , or iodine , the last being the most reactive . However , trifluoromethyl groups are unreactive towards lithium aluminium hydride . For ...
... reduction of organic halides to hydrocarbons is well known.1 The halogen may be chlorine , bromine , or iodine , the last being the most reactive . However , trifluoromethyl groups are unreactive towards lithium aluminium hydride . For ...
Contents
Page | 1 |
Electrochemical Indications of New Oxidation States in Transitionmetal Dicarbollide Complexes | 8 |
Crystal Structure and Bonding in the Dinuclear Complexes CHW SPhMCO M Cr | 14 |
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acetate acid Acta adduct alcohol alkaloids alkyl Amer analysis anion aqueous aromatic assigned atoms band benzene carbon carbonyl cation chelate Chem chemical shifts Chemical Society Chim chloride cm-¹ co-ordination Comm complexes compounds configuration confirmed coupling Crystal Structure cyclopropane Department of Chemistry derivatives double bond doublet electron ester ether Figure formation formed gave H₂O hydride hydrogen hydrolysis i.r. spectrum ibid indicate Inorg intermediate irradiation isolated isomer ketone ligand metal methanol methyl methylene mixture molecular molecule n.m.r. spectrum nitrogen observed obtained olefinic oxidation oxygen phenyl phosphine photolysis Phys presence protons pyridine radical ratio reaction rearrangement Received reported resonance ring room temperature shown shows similar singlet sodium solution solvent space group spectra spectroscopy stereochemistry studies substituted suggested sulphur Summary synthesis Table Tetrahedron Letters tetrahydrofuran tion triphenylphosphine tritium University values X-ray yield