Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
From inside the book
Results 1-3 of 78
Page
... Recently Alder et al ' have shown that 1,8- bis ( dimethylamino ) -naphthalene is a highly strained molecule whose strains are effectively relieved by protonation . It is a remarkably strong CH , CH , CH , CH , mono - acidic base with ...
... Recently Alder et al ' have shown that 1,8- bis ( dimethylamino ) -naphthalene is a highly strained molecule whose strains are effectively relieved by protonation . It is a remarkably strong CH , CH , CH , CH , mono - acidic base with ...
Page 55
... recently reported barriers in dibenzylmethylamine , 11 - dibenzylhydrazine , and NN - dibenzylhydroxylamine Table 2 ) . The AG values in Table 2 roughly parallel the inductive order of the substituent ( X ) rather than the order of ...
... recently reported barriers in dibenzylmethylamine , 11 - dibenzylhydrazine , and NN - dibenzylhydroxylamine Table 2 ) . The AG values in Table 2 roughly parallel the inductive order of the substituent ( X ) rather than the order of ...
Page 424
... Recently Nair and co - workers have deduced structure ( V ) for the pale yellow crystalline material first isolated in 19497 from a bicar- bonate extract of the leaves of Cassia reticulata Willdenow . This same compound has also been ...
... Recently Nair and co - workers have deduced structure ( V ) for the pale yellow crystalline material first isolated in 19497 from a bicar- bonate extract of the leaves of Cassia reticulata Willdenow . This same compound has also been ...
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
Other editions - View all
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 |