Quarterly Journal of the Chemical Society of London, Issue 1, Pages 1-776 |
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Page 74
2 : 1 - addition products of the quinone to SO ,. From both quinones the 1 : 1 - adducts are the corresponding sultone ( V ) and the cyclic sulphone ( VI ) , ( V ) being the major product . Moreover , from the reaction of ( Ib ) the ...
2 : 1 - addition products of the quinone to SO ,. From both quinones the 1 : 1 - adducts are the corresponding sultone ( V ) and the cyclic sulphone ( VI ) , ( V ) being the major product . Moreover , from the reaction of ( Ib ) the ...
Page 296
1,3 - Dipolar Additions of Glycosyl Azides to Substituted Acetylenes By ROBERT E. HARMON , * ROBERT A. Earl ... acetylenes afford the corresponding triazoles ( equation 1 ) .1 N R1 - C NR2 C - X ( 1 ) The addition of glycosyl azides ...
1,3 - Dipolar Additions of Glycosyl Azides to Substituted Acetylenes By ROBERT E. HARMON , * ROBERT A. Earl ... acetylenes afford the corresponding triazoles ( equation 1 ) .1 N R1 - C NR2 C - X ( 1 ) The addition of glycosyl azides ...
Page 472
Asymmetric Induction in Electrophilic Addition to aß - Unsaturated Sulphoxides By D. J. ABBOTT ( Esso Research ... 2 P. B. de la Mare and R. Bolton , " Electrophilic Additions to Unsaturated Systems , " Elsevier , London , 1966 .
Asymmetric Induction in Electrophilic Addition to aß - Unsaturated Sulphoxides By D. J. ABBOTT ( Esso Research ... 2 P. B. de la Mare and R. Bolton , " Electrophilic Additions to Unsaturated Systems , " Elsevier , London , 1966 .
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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