TEMPO/HCl/NaNO2 Catalyst: A Transition??Metal??Free Approach to Efficient Aerobic Oxidation of Alcohols to Aldehydes and Ketones Under Mild Conditions
X Wang, R Liu, Y Jin, X Liang
Index: Wang, Xinliang; Liu, Renhua; Jin, Yu; Liang, Xinmiao Chemistry - A European Journal, 2008 , vol. 14, # 9 p. 2679 - 2685
Full Text: HTML
Citation Number: 128
Abstract
Abstract Hydrochloric acid, a very inexpensive and readily available inorganic acid, has been found to cooperate exquisitely with NaNO 2/TEMPO in catalyzing the molecular- oxygen-driven oxidation of a broad range of alcohol substrates to the corresponding aldehydes and ketones. This transition-metal-free catalytic oxidative conversion is novel and represents an interesting alternative route to the corresponding carbonyl compounds to ...
Related Articles:
[New Journal of Chemistry, , vol. 31, # 2 p. 277 - 286]
Enamines from terminal epoxides and hindered lithium amides
[Journal of the American Chemical Society, , vol. 126, # 22 p. 6870 - 6871]
[Harvey, Benjamin G.; Meylemans, Heather A.; Quintana, Roxanne L. Green Chemistry, 2012 , vol. 14, # 9 p. 2450 - 2456]
Coordination Studies on Supramolecular Chiral Ligands and Application in Asymmetric Hydroformylation
[Chemistry - A European Journal, , vol. 18, # 23 p. 7091 - 7099]
Coordination Studies on Supramolecular Chiral Ligands and Application in Asymmetric Hydroformylation
[Chemistry - A European Journal, , vol. 18, # 23 p. 7091 - 7099]