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contributor authorمصطفی قلی زادهen
contributor authorMostafa Gholizadehfa
date accessioned2020-06-06T14:21:53Z
date available2020-06-06T14:21:53Z
date issued2007
identifier urihttp://libsearch.um.ac.ir:80/fum/handle/fum/3393561?show=full
description abstractP2O5 /H3PO4 (PPA) was found to be an efficient new reagent for probing the mechanism of acylation reactions and Fries rearrangement of acyloxy benzene derivatives and also the direct acylation reactions of phenol derivatives with Carboxylic acids. The reactions proceeded smoothly in the presence of PPA and are highly selective for the preparation of the ortho isomers of hydroxyaryl ketones. In the same way we have investigated the effects of ortho, meta and para substituents on the acylation reactions of benzoic acid derivatives and also Fries rearrangement in PPA.en
languageEnglish
titleA study of probing the mechanism of acylation Reactions and Fries Rearrangement by Polyphosphoric acid (PPA(en
typeJournal Paper
contenttypeExternal Fulltext
subject keywordsPolyphosphoric acid (PPA)en
subject keywordsAcylation reactionsen
subject keywordsFries rearrangementen
subject keywordsHydroxyaryl Ketonesen
subject keywordsPhenol derivativesen
journal titleInternational Journal of Applied Chemistryen
journal titleInternational Journal of Applied Chemistryfa
pages1-Jan
journal volume1
journal issue1
identifier linkhttps://profdoc.um.ac.ir/paper-abstract-1014760.html
identifier articleid1014760


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