Nucleophilic Displacement Reactions at the Thiolester Bond. III.1Kinetic Demonstration of Metastable Intermediates in the Hydroxylaminolysis and Methoxylaminolysis of Thiolesters and Thiolactones in Aqueous Solutions

1964 ◽  
Vol 86 (22) ◽  
pp. 4886-4897 ◽  
Author(s):  
Thomas C. Bruice ◽  
Leo R. Fedor



1981 ◽  
Vol 59 (15) ◽  
pp. 2412-2416 ◽  
Author(s):  
John A. Stone ◽  
Margaret S. Lin ◽  
Jeffrey Varah

The reactivity of the dimethylchloronium ion with a series of aromatic hydrocarbons has been studied in a high pressure mass spectrometer ion source using the technique of reactant ion monitoring. Benzene is unreactive but all others, from toluene to mesitylene, react by CH3+ transfer to yield σ-bonded complexes. The relative rate of reaction increases with increasing exothermicity in line with current theories of nucleophilic displacement reactions.



Tetrahedron ◽  
2003 ◽  
Vol 59 (6) ◽  
pp. 789-794 ◽  
Author(s):  
Nuno M.T Lourenço ◽  
Carlos A.M Afonso


1982 ◽  
Vol 47 (22) ◽  
pp. 4388-4389 ◽  
Author(s):  
Samuel P. McManus ◽  
Kamellia Kamkar Safavy ◽  
F. Ellen Roberts


Sign in / Sign up

Export Citation Format

Share Document