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 |
Synthesis of a 1026Pyridinophane by U K GEORGI and J RÉTEY | 32 |
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acetate acid addition alcohol Amer analysis appears aromatic assigned atoms band bond calculated carbon carbonyl Chem Chemical Chemistry chloride chromatography co-ordination Comm complexes compounds concentration configuration confirmed consistent constants containing corresponding coupling Crystal Department of Chemistry derivatives determined effect electron ester ether evidence expected experiments Figure followed formation formed gave give hydrogen indicate intermediate involving isolated ligand mass measured mechanism metal method methyl mixture molecular molecule n.m.r. spectrum nitrogen observed obtained occurs oxidation oxygen peak position possible prepared presence protons radical ratio reaction rearrangement Received recently reduction relative reported Research resonance respectively ring Scheme shift shown shows signals similar solution solvent space group spectra spectrum structure studies substituted suggested Summary synthesis Table temperature Tetrahedron Letters thank tion University values X-ray yield