Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 1
... presence of acetate ions , as a route to arynes , becomes clear . The unique success , even in the presence of water , in the o - t - butyl case3 can be attributed to the difference in timing of the loss of nitrogen from the diazonium ...
... presence of acetate ions , as a route to arynes , becomes clear . The unique success , even in the presence of water , in the o - t - butyl case3 can be attributed to the difference in timing of the loss of nitrogen from the diazonium ...
Page 247
... presence of ligands such as triphenylphosphine . HYDROSILATION of olefins is catalysed by transition - metal empounds , platinum compounds being especially widely However palladium compounds are regarded as nactive for hydrosilation ...
... presence of ligands such as triphenylphosphine . HYDROSILATION of olefins is catalysed by transition - metal empounds , platinum compounds being especially widely However palladium compounds are regarded as nactive for hydrosilation ...
Page 330
... presence of palladium complexes is very slow and yields only octa- trienes . When the reaction was run in the presence of solvents such as t - butyl alcohol , acetone , or acetonitrile , the reaction was still slow giving octa - 1,3,7 ...
... presence of palladium complexes is very slow and yields only octa- trienes . When the reaction was run in the presence of solvents such as t - butyl alcohol , acetone , or acetonitrile , the reaction was still slow giving octa - 1,3,7 ...
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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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 |