Nucleophilic Displacement Reactions in Ionic Liquids:  Substrate and Solvent Effect in the Reaction of NaN3and KCN with Alkyl Halides and Tosylates†

2003 ◽  
Vol 68 (17) ◽  
pp. 6710-6715 ◽  
Author(s):  
Cinzia Chiappe ◽  
Daniela Pieraccini ◽  
Paola Saullo

ChemInform ◽  
2010 ◽  
Vol 32 (36) ◽  
pp. no-no
Author(s):  
Christy Wheeler ◽  
Kevin N. West ◽  
Charles L. Liotta ◽  
Charles A. Eckert


2001 ◽  
pp. 887-888 ◽  
Author(s):  
Christy Wheeler ◽  
Kevin N. West ◽  
Charles A. Eckert ◽  
Charles L. Liotta




2004 ◽  
Vol 2004 (4) ◽  
pp. 276-278 ◽  
Author(s):  
Yi Hu ◽  
Zhen-Chu Chen ◽  
Zhang-Gao Le ◽  
Qin-Guo Zheng


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


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