Publication:
Reactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative study

Simple item page
dc.contributor.authorWanchai Pluempanupaten_US
dc.contributor.authorOraphin Chantarasriwongen_US
dc.contributor.authorPiyada Taboonpongen_US
dc.contributor.authorDoo Ok Jangen_US
dc.contributor.authorWarinthorn Chavasirien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherYonsei University Wonju Campusen_US
dc.date.accessioned2018-08-24T01:43:50Z
dc.date.available2018-08-24T01:43:50Z
dc.date.issued2007-01-08en_US
dc.description.abstractThe reactivity of chlorinating agents was examined with the aid of1H NMR using competitive reactions between selected chlorinating agents and CBr4towards alcohols and carboxylic acids. The reactivity was greatly dependent on the type of substituent on the chlorinating agents. COCCl3and CN substituted trichloromethyl groups enhanced the reactivity of the chlorinating agent with PPh3for the chlorination of alcohols and carboxylic acids. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.48, No.2 (2007), 223-226en_US
dc.identifier.doi10.1016/j.tetlet.2006.11.060en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-33845221264en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/24267
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845221264&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleReactivity of chlorinating agents/PPh<inf>3</inf>for the chlorination of alcohols and carboxylic acids: a comparative studyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845221264&origin=inwarden_US

Files

Collections

Scopus 2006-2010