Please use this identifier to cite or link to this item: http://idr.nitk.ac.in/jspui/handle/123456789/12968
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dc.contributor.authorDileep, R.
dc.contributor.authorBhat, B.R.
dc.contributor.authorKumara, T.H.S.
dc.date.accessioned2020-03-31T08:42:33Z-
dc.date.available2020-03-31T08:42:33Z-
dc.date.issued2014
dc.identifier.citationGreen Chemistry Letters and Reviews, 2014, Vol.7, 1, pp.32-36en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/12968-
dc.description.abstractPalladium (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]PF6 with an equal-proportioned CH2Cl2 than in the single CH2Cl2 or IL. 2014 The Author(s). Published by Taylor &ampen_US
dc.titlePalladium complex in a room temperature ionic liquid: A convenient recyclable reagent for catalytic oxidationen_US
dc.typeArticleen_US
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