Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 278
... shown in Figure 1 , together with the representation of the major rotamers . From expanded scale spectra of the proton groups shown in Figure 1 , the vicinal proton - proton coupling constant Ĵ was measured as a function of temperature ...
... shown in Figure 1 , together with the representation of the major rotamers . From expanded scale spectra of the proton groups shown in Figure 1 , the vicinal proton - proton coupling constant Ĵ was measured as a function of temperature ...
Page 408
... shown on an expanded scale in Figure ( 2a ) . four equidistant peaks are clearly shown , with an overlap occurring with the first peak of each set . This double set of peaks arises from the hyperfine interaction of the un- paired ...
... shown on an expanded scale in Figure ( 2a ) . four equidistant peaks are clearly shown , with an overlap occurring with the first peak of each set . This double set of peaks arises from the hyperfine interaction of the un- paired ...
Page 432
... shown , and ( 1 ) and ( 2 ) and related sesquiter- penoids would be expected to have cis - fused hydrindane skeletons . To test this hypothesis we have determined the crystal structures of a pair of illudol and marasmic acid derivatives ...
... shown , and ( 1 ) and ( 2 ) and related sesquiter- penoids would be expected to have cis - fused hydrindane skeletons . To test this hypothesis we have determined the crystal structures of a pair of illudol and marasmic acid derivatives ...
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
Bibliographic information
| Title | Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
| Author | Chemical Society (Great Britain) |
| Contributor | Royal Society of Chemistry (Great Britain) |
| Published | 1971 |
| Original from | the University of Michigan |
| Digitized | 22 Mar 2006 |
| Export Citation | BiBTeX EndNote RefMan |