Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands

The microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine with various unprotected amino acids was developed for the synthesis of C 3-symmetrical polycarboxylate ligands which can be used as structural directing units in metal-organic f...

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Main Authors: Karuehanon W., Fanfuenha W., Rujiwatra A., Pattarawarapan M.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84861054515&partnerID=40&md5=f52c8214810def7f204acc775666093a
http://cmuir.cmu.ac.th/handle/6653943832/6662
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Language: English
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spelling th-cmuir.6653943832-66622014-08-30T03:51:04Z Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands Karuehanon W. Fanfuenha W. Rujiwatra A. Pattarawarapan M. The microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine with various unprotected amino acids was developed for the synthesis of C 3-symmetrical polycarboxylate ligands which can be used as structural directing units in metal-organic frameworks. The reactions were performed in water using a domestic microwave oven as the heating device. In comparison to the reactions performed under conventional heating, the reactions under microwave irradiation proceeded much more rapidly within 20 min to afford the desired ligands in comparative yields to those obtained by conventional heating. © 2012. 2014-08-30T03:51:04Z 2014-08-30T03:51:04Z 2012 Article in Press 00404039 10.1016/j.tetlet.2012.04.124 TELEA http://www.scopus.com/inward/record.url?eid=2-s2.0-84861054515&partnerID=40&md5=f52c8214810def7f204acc775666093a http://cmuir.cmu.ac.th/handle/6653943832/6662 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description The microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine with various unprotected amino acids was developed for the synthesis of C 3-symmetrical polycarboxylate ligands which can be used as structural directing units in metal-organic frameworks. The reactions were performed in water using a domestic microwave oven as the heating device. In comparison to the reactions performed under conventional heating, the reactions under microwave irradiation proceeded much more rapidly within 20 min to afford the desired ligands in comparative yields to those obtained by conventional heating. © 2012.
format Article
author Karuehanon W.
Fanfuenha W.
Rujiwatra A.
Pattarawarapan M.
spellingShingle Karuehanon W.
Fanfuenha W.
Rujiwatra A.
Pattarawarapan M.
Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
author_facet Karuehanon W.
Fanfuenha W.
Rujiwatra A.
Pattarawarapan M.
author_sort Karuehanon W.
title Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
title_short Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
title_full Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
title_fullStr Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
title_full_unstemmed Microwave-assisted S NAr reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of C 3-symmetrical polycarboxylate ligands
title_sort microwave-assisted s nar reaction of 2,4,6-trichloro-1,3,5-triazine for the rapid synthesis of c 3-symmetrical polycarboxylate ligands
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84861054515&partnerID=40&md5=f52c8214810def7f204acc775666093a
http://cmuir.cmu.ac.th/handle/6653943832/6662
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