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dc.contributor.authorWatcharee Funfuenhaen_US
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-04T09:44:48Z-
dc.date.available2018-09-04T09:44:48Z-
dc.date.issued2014-09-02en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-84949124339en_US
dc.identifier.other10.1016/j.tet.2014.06.127en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84949124339&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53182-
dc.description.abstract© 2014 Elsevier Ltd. All rights reserved. A rapid and efficient method for preparation of C2-symmetrical 1,3,5-triazine polycarboxylate ligands was developed. The reactions included either selective mono- or di-substitution of 2,4,6-trichloro-1,3,5-triazine with various nucleophiles containing carboxyl group(s), followed by nucleophilic displacement of the remained chloride(s) in aqueous media under microwave irradiation. Novel C2-symmetrical tripodal ligands were afforded in good yields and purities under short reaction time with simple work-up, which are potentially useful as structural directing units in metal-organic frameworks.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFacile and efficient synthesis of C<inf>2</inf>-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiationen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedronen_US
article.volume70en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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