Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 6
We thank the Petroleum Research Fund of the American Chemical Society for partial support of this work . ( Received , October 19th , 1970 ; Com . 1800. ) 1 E. W. Schlag and B. S. Rabinovitch , J. Amer . Chem .
We thank the Petroleum Research Fund of the American Chemical Society for partial support of this work . ( Received , October 19th , 1970 ; Com . 1800. ) 1 E. W. Schlag and B. S. Rabinovitch , J. Amer . Chem .
Page 383
We use the terminology " face - to - face , " " face - to - edge , " and " edge - to - edge " ( E. W. Yankee and D.J. Cram , J. Amer . Chem . Soc . , 1970 , 92 , 6331 ) to describe the three different limiting diradical entities in ...
We use the terminology " face - to - face , " " face - to - edge , " and " edge - to - edge " ( E. W. Yankee and D.J. Cram , J. Amer . Chem . Soc . , 1970 , 92 , 6331 ) to describe the three different limiting diradical entities in ...
Page 510
Soc . , 1959 , 2384 . d This work . e H. C. Brown and X. R. Mihm , J. Amer . Chem . Soc . , 1955 , 77 , 1723 . K. Schofield , ' Heteroaromatic Nitrogen Compounds , ' Butterworths , London , 1967 , page 325 , quotes log Ku as Mason and ...
Soc . , 1959 , 2384 . d This work . e H. C. Brown and X. R. Mihm , J. Amer . Chem . Soc . , 1955 , 77 , 1723 . K. Schofield , ' Heteroaromatic Nitrogen Compounds , ' Butterworths , London , 1967 , page 325 , quotes log Ku as Mason and ...
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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