Quarterly Journal of the Chemical Society of London, Issue 15, Pages 777-1692 |
From inside the book
Results 1-3 of 78
Page 843
... catalysts described above . It was noted above that the results indicated no ligand exchange during the course of the reaction when 2-3 mol % of catalyst was used . This hypothesis was supported by experiments in which the catalyst ...
... catalysts described above . It was noted above that the results indicated no ligand exchange during the course of the reaction when 2-3 mol % of catalyst was used . This hypothesis was supported by experiments in which the catalyst ...
Page 1180
... catalyst or catalyst plus peroxide . After 24 h at reflux , the excess of olefin was removed by distillation , and the residue analysed by g.l.c. using diglyme as an internal standard . E. I. du Pont de Nemours and Company , trademark ...
... catalyst or catalyst plus peroxide . After 24 h at reflux , the excess of olefin was removed by distillation , and the residue analysed by g.l.c. using diglyme as an internal standard . E. I. du Pont de Nemours and Company , trademark ...
Page 1203
... catalyst with halogenated species Initial rate ( Nm - 2 min - 1 ) R. L. Banks and G. C. Bailey , Ind . and Eng . Chem . ( Product Res . and Development ) , 1963 , 3 , 170 . E. S. Davie , D. A. Whan , and C. Kemball , J. Catalysis , in ...
... catalyst with halogenated species Initial rate ( Nm - 2 min - 1 ) R. L. Banks and G. C. Bailey , Ind . and Eng . Chem . ( Product Res . and Development ) , 1963 , 3 , 170 . E. S. Davie , D. A. Whan , and C. Kemball , J. Catalysis , in ...
Contents
11 August 1971 | 777 |
Electron Spin Resonance Studies of Stable Radicals Generated by Oxidation of sButyllithium with Transition | 878 |
O COPYRIGHT 1971 | 1044 |
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Common terms and phrases
absorption acetate acid Acta adduct alcohol alkaloids alkyl Amer angle anion aqueous aromatic atoms bands benzene carbon carbonyl catalyst cation CH₂ Chem chemical shifts Chemical Society Chim chloride cm-¹ co-ordination Comm complex compounds corresponding Crystal cyclic cyclopropyl D. H. R. BARTON Department of Chemistry derivatives deuterium dimethyl electron ester ether Figure formation formed gave give hydrogen hydrolysis i.r. spectrum ibid Inorg intermediate irradiation isolated isomer isomeric ketone ligand mechanism metal methanol methyl methylene mixture molecular molecule n.m.r. spectrum nitrogen nucleophilic observed obtained olefin orbitals oxidation oxygen Ph Ph phenyl phosphine photolysis Phys presence protons pyridine radical ratio react reaction rearrangement Received reduction reported resonance ring room temperature shown singlet sodium solution solvent species spectra spectroscopy stereochemistry structure studies substituted Summary synthesis Table Tetrahedron Letters thermal University X-ray yield