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dc.contributor.authorTheodorou, V.en
dc.contributor.authorSkobridis, K.en
dc.contributor.authorTzakos, A. G.en
dc.contributor.authorRagoussis, V.en
dc.date.accessioned2015-11-24T16:38:39Z-
dc.date.available2015-11-24T16:38:39Z-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8066-
dc.rightsDefault Licence-
dc.subjectsaponification of estersen
dc.subjectmechanismen
dc.subjectnon-aqueous conditionsen
dc.subjectmethanolysisen
dc.subjectselective enrichment of coohen
dc.subjectcarboxylic acidsen
dc.subjectalcoholsen
dc.subjecttransition-stateen
dc.subjectsaponificationen
dc.subjectconvenienten
dc.subjecthydroxideen
dc.subjectmicrowaveen
dc.subjectcarbonylen
dc.subjectacetateen
dc.subjectphaseen
dc.subjectacidsen
dc.subjectbaseen
dc.titleA simple method for the alkaline hydrolysis of estersen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.tetlet.2007.09.074-
heal.identifier.secondary<Go to ISI>://000252097100035-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040403907018539/1-s2.0-S0040403907018539-main.pdf?_tid=d6cb09dc-3a30-11e3-9880-00000aacb360&acdnat=1382346898_c69e29369395a174d8b8a2b61b5b2c3d-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2007-
heal.abstractA very mild and rapid procedure for the efficient alkaline hydrolysis of esters in non-aqueous conditions has been developed, by the use of dichloromethane/methanol (9:1) as solvent. This method conveniently provides both carboxylic acids and alcohols from the corresponding esters and sodium hydroxide in a few minutes at room temperature. A plausible reaction mechanism is proposed. (C) 2007 Elsevier Ltd. All rights reserved.en
heal.publisherElsevieren
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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