Background
Type: Article

Convenient transformation of thiocarbonyl to carbonyl group using benzyltriphenylphosphonium and n-butyltriphenylphosphonium peroxodisulfates

Journal: Journal of Chemical Research - Part S (03082342)Year: 2003/06/01Volume: Issue: 6
Mohammadpoor Baltork I.a Sadeghi M.M.M. Esmayilpour K.
BronzeDOI:10.3184/030823403103174074Language: English

Abstract

Benzyltriphenylphosphonium and n-butyltriphenylphosphonium peroxodisulfates are stable and easily prepared oxidising agents. These reagents are able to convert different thioamides and thioureas to their oxygen analogues in good to excellent yields. Thiono esters are also transformed to esters in high yields. Thioketones such as thiobenzophenone and thiofluorenone are converted to their ketones in high yields while, 4-nitrothiobenzophenone, 2-aminothiobenzophenone and 4-chlorothiobenzophenone remained intact in the reaction mixture.


Author Keywords

Carbonyl compounsPeroxodisulfateThiocarbonyl2 aminothiobenzophenone4 chlorothiobenzophenone4 nitrothiobenzophenonebenzophenone derivativebenzyltriphenylphosphoniumcarbonyl derivativeester derivativefluorenone derivativeketonen butyltriphenylphosphonium peroxodisulfateoxidizing agentoxygenphosphonium derivativethioamidethiobenzophenonethiocarbonyl derivativethiofluorenonethioketonethiono esterthioureaunclassified drug