Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 139
... carbon - carbon double bond , see M. Calvin and R. E. Buckles , J. Amer . Chem . Soc . , 1940 , 62 , 3324 ; ( b ) S. M. McElvain , Chem . Rev. , 1945 , 45 , 453 ; ( c ) Y. Shvo , Tetrahedron Letters , 1968 , 5923 ; ( d ) See H. Kessler ...
... carbon - carbon double bond , see M. Calvin and R. E. Buckles , J. Amer . Chem . Soc . , 1940 , 62 , 3324 ; ( b ) S. M. McElvain , Chem . Rev. , 1945 , 45 , 453 ; ( c ) Y. Shvo , Tetrahedron Letters , 1968 , 5923 ; ( d ) See H. Kessler ...
Page 330
... carbon dioxide . + H2O + CO2 Pd ( acac ) 2 , PPh3 OH + ( 1 ) ( II ) OH octadienyl ethers ( IV ) Table 1 shows the high yields of octadienols obtained in the carbon dioxide - assisted reaction in various solvents TABLE 1 Synthesis of ...
... carbon dioxide . + H2O + CO2 Pd ( acac ) 2 , PPh3 OH + ( 1 ) ( II ) OH octadienyl ethers ( IV ) Table 1 shows the high yields of octadienols obtained in the carbon dioxide - assisted reaction in various solvents TABLE 1 Synthesis of ...
Page 400
... carbon . Value shown is for methyl carbon . 8 Solution in CDCI ,. C - I 142.8 H → CH NO Me 30.9 Me Si JAY FIGURE . 13C " Fourier " power spectrum of N - methyl - N - nitroso- aniline at 22.63 MHz measured as a " neat " liquid ...
... carbon . Value shown is for methyl carbon . 8 Solution in CDCI ,. C - I 142.8 H → CH NO Me 30.9 Me Si JAY FIGURE . 13C " Fourier " power spectrum of N - methyl - N - nitroso- aniline at 22.63 MHz measured as a " neat " liquid ...
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 |
15 other sections not shown
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Common terms and phrases
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 |