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DC Field | Value | Language |
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dc.contributor.author | Watcharee Funfuenha | en_US |
dc.contributor.author | Wong Phakhodee | en_US |
dc.contributor.author | Mookda Pattarawarapan | en_US |
dc.date.accessioned | 2018-09-04T09:44:48Z | - |
dc.date.available | 2018-09-04T09:44:48Z | - |
dc.date.issued | 2014-09-02 | en_US |
dc.identifier.issn | 14645416 | en_US |
dc.identifier.issn | 00404020 | en_US |
dc.identifier.other | 2-s2.0-84949124339 | en_US |
dc.identifier.other | 10.1016/j.tet.2014.06.127 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84949124339&origin=inward | en_US |
dc.identifier.uri | http://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.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Facile and efficient synthesis of C<inf>2</inf>-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Tetrahedron | en_US |
article.volume | 70 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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