Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation

© 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 carbo...

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Main Authors: Funfuenha,W., Phakhodee,W., Pattarawarapan,M.
Format: Article
Published: Elsevier Limited 2015
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http://cmuir.cmu.ac.th/handle/6653943832/38759
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spelling th-cmuir.6653943832-387592015-06-16T07:54:09Z Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation Funfuenha,W. Phakhodee,W. Pattarawarapan,M. Drug Discovery Organic Chemistry Biochemistry © 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. 2015-06-16T07:54:09Z 2015-06-16T07:54:09Z 2014-01-01 Article 00404020 2-s2.0-84906084159 10.1016/j.tet.2014.06.127 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84906084159&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38759 Elsevier Limited
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Drug Discovery
Organic Chemistry
Biochemistry
spellingShingle Drug Discovery
Organic Chemistry
Biochemistry
Funfuenha,W.
Phakhodee,W.
Pattarawarapan,M.
Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
description © 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.
format Article
author Funfuenha,W.
Phakhodee,W.
Pattarawarapan,M.
author_facet Funfuenha,W.
Phakhodee,W.
Pattarawarapan,M.
author_sort Funfuenha,W.
title Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_short Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_full Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_fullStr Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_full_unstemmed Facile and efficient synthesis of C2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
title_sort facile and efficient synthesis of c2-symmetrical 1,3,5-triazine polycarboxylate ligands under microwave irradiation
publisher Elsevier Limited
publishDate 2015
url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84906084159&origin=inward
http://cmuir.cmu.ac.th/handle/6653943832/38759
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