Dileep, R.Badekai Ramachandra, B.Suresha Kumara, T.H.S.2026-02-052014Green Chemistry Letters and Reviews, 2014, 7, 1, pp. 32-3617518253https://doi.org/10.1080/17518253.2014.891660https://idr.nitk.ac.in/handle/123456789/26646Palladium (Pd)-catalyzed carbonylation of alcohols proceeds in ionic liquid (IL) media (1-ethyl-3-methylimidazolium hexafluorophosphate). Carbonylation of primary/secondary alcohols to aldehydes/ketones was greatly accelerated by the use of a Pd-based catalyst in the presence of NaOCl as an oxidant. The catalyst was more easier to recycle in the IL [Emim]PF<inf>6</inf> with an equal-proportioned CH<inf>2</inf>Cl<inf>2</inf> than in the single CH<inf>2</inf>Cl<inf>2</inf> or IL. © 2014 The Author(s). Published by Taylor & Francis.alcoholaldehydecatalysiscatalystketoneoxidationpalladiumreaction kineticstemperature effect