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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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 |
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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 |
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© 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 |
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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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1681421531787296768 |