Publication:
Synthesis of unsymmetrical benzil licoagrodione

Simple item page
dc.contributor.authorRattana Worayuthakarnen_US
dc.contributor.authorSasiwadee Boonya-udtayanen_US
dc.contributor.authorEakarat Arom-oonen_US
dc.contributor.authorPoonsakdi Ploypradithen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.authorNopporn Thasanaen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherChulabhorn Graduate Instituteen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-07-12T02:22:16Z
dc.date.available2018-07-12T02:22:16Z
dc.date.issued2008-09-19en_US
dc.description.abstract(Chemical Equation Presented) A synthesis of unsymmetrical 1,2-diarylethane-1,2-dione is reported involving the intramolecular cyclization of anionic benzylic ester of the aryl benzyl ether followed by oxidation employing dioxirane. With the use of microwave irradiation, licoagrodione was prepared from Claisen rearrangement of the corresponding allyl phenyl ether 1,2-diketone readily available from the Lindlar's reduction of the corresponding alkyne derivative. Subsequent removal of protecting groups then furnished the desired product. © 2008 American Chemical Society.en_US
dc.identifier.citationJournal of Organic Chemistry. Vol.73, No.18 (2008), 7432-7435en_US
dc.identifier.doi10.1021/jo8013353en_US
dc.identifier.issn00223263en_US
dc.identifier.other2-s2.0-52449127988en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/19064
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=52449127988&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleSynthesis of unsymmetrical benzil licoagrodioneen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=52449127988&origin=inwarden_US

Files

Collections

Scopus 2006-2010