Oxidative N-Dealkylation of Tertiary Amines with Tetraethylammonium Periodate Catalyzed by Metal Complexes

2017 ◽  
Vol 70 (3) ◽  
pp. 233 ◽  
Author(s):  
Daisy Bhat ◽  
Nidhi Sharma

The oxidative N-dealkylation of tertiary amines, N,N-dimethylaniline and N,N-diethylaniline, catalyzed by some sterically hindered FeIII complexes and tetraethylammonium periodate as oxidant gave the corresponding N-dealkylated and mono-oxygenated products in good yields. The presence of electronegative atoms on the catalyst complexes influenced the product yield. The presence of H-atom abstractor 2,6-di-tert-butyl-4-methylphenol did not influence product formation, thereby suggesting that the reaction proceeded predominantly via a one-electron transfer mechanism rather than via hydrogen abstraction. Tetraethylammonium periodate favoured oxygen transfer to the substrate.

2015 ◽  
Vol 14 (3) ◽  
pp. 563-568 ◽  
Author(s):  
Theodoros S. Symeonidis ◽  
Ioannis Tamiolakis ◽  
Gerasimos S. Armatas ◽  
Ioannis N. Lykakis

Decatungstate supported on mesoporous TiO2 nanoparticle assemblies catalyze the selective and efficient oxidation of aromatic alcohols under “green” oxidation conditions. An electron transfer mechanism was predominated under UV-vis irradiation.


1987 ◽  
Vol 65 (5) ◽  
pp. 976-979 ◽  
Author(s):  
Philip A. Carson ◽  
Paul de Mayo

1,2-Diphenylcyclopropane (1) was found to be oxidized on illuminated ZnO in the presence of air while 1-(p-methoxyphenyl)-2-phenylcyclopropane (2) and 1,2-bis(p-methoxyphenyl)cyclopropane (3) were found to be similarly oxidized on illuminated CdS. Compounds 2 and 3 were found, also, to undergo a rapid photochemical cis-trans isomerization on CdS whereas 1 did not undergo such isomerization. An electron transfer mechanism involving formation of the radical cations of the substrates is proposed.


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