Activated aromatic substitution by piperidine or [1-2H]piperidine in benzene. Dependence of kinetic deuterium isotope effect on the group displaced

Author(s):  
Francesco Pietra ◽  
Dario Vitali ◽  
Sergio Frediani
1963 ◽  
Vol 41 (12) ◽  
pp. 3127-3131 ◽  
Author(s):  
R. A. Abramovitch ◽  
Choo-Seng Giam

The ratios of isomers formed in the reaction of 3-alkylpyridines with phenyllithium under various conditions appear to be invariant within the limits of experimental error. A number of experiments, including the reaction of phenyllithium with 3-picoline-2d and with an excess of a mixture of pyridine and pyridine-2d, are described which establish that the hydride ion elimination stage in these nucleophilic aromatic substitutions is not important in determining the observed orientation and that the addition stage is either virtually irreversible or that the equilibrium lies far on the product side and is not rapidly reversible. A convenient new procedure is described for working up the reaction mixtures.


1991 ◽  
Vol 0 (12) ◽  
pp. 801-802 ◽  
Author(s):  
Panayiotis Anastasis ◽  
Raymond Duffin ◽  
Christopher Gilmore ◽  
Karl Overton

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