Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 355
... mechanism involving concerted elimination of alcohol with resultant formation of substituted ketens as reactive intermediates . RECENT publication1 of evidence for an elimination- addition ( ElcB ) mechanism for hydrolysis of certain ...
... mechanism involving concerted elimination of alcohol with resultant formation of substituted ketens as reactive intermediates . RECENT publication1 of evidence for an elimination- addition ( ElcB ) mechanism for hydrolysis of certain ...
Page 380
... mechanism . LITHIUM aluminium hydride is known to reduce organic halogen compounds to the corresponding hydrocarbons . Two mechanisms have been suggested for this reaction : Eliel1 and Cram and Rickborn3 claimed it proceeded by an S2 ...
... mechanism . LITHIUM aluminium hydride is known to reduce organic halogen compounds to the corresponding hydrocarbons . Two mechanisms have been suggested for this reaction : Eliel1 and Cram and Rickborn3 claimed it proceeded by an S2 ...
Page 731
... mechanism predicting cation - solvent exchange as the slow step , cannot be the controlling mechanism in lanth- anoid complexation reactions . In recent years , complexation reactions of the lanthanoid- ( 111 ) ions have been used as a ...
... mechanism predicting cation - solvent exchange as the slow step , cannot be the controlling mechanism in lanth- anoid complexation reactions . In recent years , complexation reactions of the lanthanoid- ( 111 ) ions have been used as a ...
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