An efficient procedure for the TEMPO-catalyzed oxidation of alcohols to aldehydes and ketones using ferric chloride hexahydrate as terminal oxidant

2008 ◽  
Vol 86 (7) ◽  
pp. 720-725 ◽  
Author(s):  
R Senthil Kumar ◽  
K Karthikeyan ◽  
Paramasivan T Perumal
Keyword(s):  
Ferric Chloride ◽  
High Yield ◽  
Efficient Procedure ◽  
Chloride Hexahydrate ◽  
Oxidation Of Alcohols ◽  
Aldehydes And Ketones ◽  
Ferric Chloride Hexahydrate ◽  
Catalyzed Oxidation

A simple, efficient procedure for the oxidation of alcohols by catalytic 2,2,6,6-tetramethyl-piperidyl-1-oxy (TEMPO) was developed using FeCl3·6H2O as the terminal oxidant. The reaction gives high yield of the corresponding aldehydes and ketones with no over oxidation to the acid.Key words: oxidation, TEMPO, FeCl3·6H2O.

ChemInform Abstract: Quinazolines. Part 4. Acylation of Quinazoline-2,4-diones with Aromatic Acids Chlorides in the Presence of Ferric Chloride Hexahydrate.

ChemInform ◽  
2011 ◽  
Vol 42 (32) ◽  
pp. no-no
Author(s):  
R. Sh. Kuryazov ◽  
Yu. R. Takhirov ◽  
D. A. Dushamov ◽  
N. S. Mukhamedov ◽  
K. K. Turgunov ◽  
...  
Keyword(s):  
Ferric Chloride ◽  
Aromatic Acids ◽  
Chloride Hexahydrate ◽  
Ferric Chloride Hexahydrate

Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me3SiOOSiMe3

1983 ◽  
Vol 24 (21) ◽  
pp. 2185-2188 ◽  
Author(s):  
Shigekazu Kanemoto ◽  
Koichiro Oshima ◽  
Seijiro Matsubara ◽  
Kazuhiko Takai ◽  
Hitosi Nozaki
Keyword(s):  
Transition Metal ◽  
Oxidation Of Alcohols ◽  
Aldehydes And Ketones ◽  
Metal Catalyzed Oxidation ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed ◽  
Catalyzed Oxidation
Sign in / Sign up

Export Citation Format

Share Document