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Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid.

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dc.contributor.authorPakorn Bovonsombaten_US
dc.contributor.authorJuthamard Leykajarakulen_US
dc.contributor.authorChiraphorn Khanen_US
dc.contributor.authorKawin Pla-onen_US
dc.contributor.authorMichael M.en_US
dc.contributor.authorPratheep Khanthapuraen_US
dc.contributor.authorRameez Alien_US
dc.contributor.authorNiran Doowaen_US
dc.contributor.otherMahidol University. Mahidol University International College. Science Division.en_US
dc.date.accessioned2015-07-09T09:25:11Z
dc.date.accessioned2018-04-10T04:36:43Z
dc.date.available2015-07-09T09:25:11Z
dc.date.available2018-04-10T04:36:43Z
dc.date.created2015
dc.date.issued2009
dc.description.abstractMild and highly regioselective monoiodination of phenol and analogues is achieved in high to excellent yields at room temperature with a combination of stoichiometric p-toluenesulfonic acid and N-iodosuccinimide.en_US
dc.identifier.citationTetrahedron Letters. Vol. 50, No. 22 (2009), 2664-2667en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/10511
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.rights.holderScienceDirecten_US
dc.subjectN-iodosuccinimideen_US
dc.subjectP-toluenesulfonic aciden_US
dc.subjectRegioselective iodination of phenolen_US
dc.subjectAnaloguesen_US
dc.titleRegioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid.en_US
dspace.entity.typePublication
mods.location.urlhttp://www.sciencedirect.com/science/article/pii/S0040403909006601#
mods.location.urlhttp://ac.els-cdn.com/S0040403909006601/1-s2.0-S0040403909006601-main.pdf?_tid=287e6288-261b-11e5-b10a-00000aab0f02&acdnat=1436433559_80d1ed365a4c382ac7e98a21eee89f18

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