58418-60-3Relevant articles and documents
Pyridinium oxidations of benzyl alcohol under microwave-assisted retro-ene conditions
Jensen, Anton W.,Moore, John M.,Kimble, MaryEllen V.,Ausmus, Alex P.,Dilling, Wendell L.
supporting information, p. 5636 - 5638 (2016/11/28)
Benzyl alcohol is oxidized to benzaldehyde when heated in sulfolane in the presence of N-benzylnicotinamide and N-benzylpyridinium salts. The oxidation is accelerated in the presence microwaves. Oxidations with related pyridiniums suggest that these oxidations could occur via retro-ene reactions.
Synthesis of alkyl heteryl ethers from acetates under interphase catalysis conditions in a liquid/solid system
Abele,Abele,Gaukhman,Lukevics
, p. 40 - 43 (2007/10/03)
The reaction of acetates of heterocyclic alcohols with alkyl halides in the two-phase catalytic system of solid KOH/C6H6/18-crown-6 at room temperature leads selectively to the formation of the corresponding heterocyclic ethers in 32-93% yield. 1998 Plenum Publishing Corporation.