Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 64
... expected adduct , possessing an extended conjugated system between the enamine and the nitroso - group . Such conjugated systems may hydrolyse under the photolysis condition in the expected manner to give an a - diketone oxime ( 2 ) ...
... expected adduct , possessing an extended conjugated system between the enamine and the nitroso - group . Such conjugated systems may hydrolyse under the photolysis condition in the expected manner to give an a - diketone oxime ( 2 ) ...
Page 218
... expected for a 1,2 - trans - configuration . Close examination , however , suggests 10-20 % of 1,2 - cis - isomer may be present . Ethyl E - 2 , E - 6 - farnesoate and phenyl 3 - methylbut - 2 - enyl sulphone similarly gave ( Va ) ( 50 ...
... expected for a 1,2 - trans - configuration . Close examination , however , suggests 10-20 % of 1,2 - cis - isomer may be present . Ethyl E - 2 , E - 6 - farnesoate and phenyl 3 - methylbut - 2 - enyl sulphone similarly gave ( Va ) ( 50 ...
Page 492
... expected for Cr ( H2O ) s ( O2CCH2SH ) 2 + . At low acid concentrations this complex reverts back to the +1 ion . The interconversion together with the spectrophoto- metrically determined rate law at constant acidity can be described by ...
... expected for Cr ( H2O ) s ( O2CCH2SH ) 2 + . At low acid concentrations this complex reverts back to the +1 ion . The interconversion together with the spectrophoto- metrically determined rate law at constant acidity can be described by ...
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