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DC Field | Value | Language |
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dc.contributor.author | Pingaew R. | |
dc.contributor.author | Prachayasittikul S. | |
dc.contributor.author | Ruchirawat S. | |
dc.contributor.author | Prachayasittikul V. | |
dc.date.accessioned | 2021-04-05T03:32:48Z | - |
dc.date.available | 2021-04-05T03:32:48Z | - |
dc.date.issued | 2013 | |
dc.identifier.issn | 10018417 | |
dc.identifier.other | 2-s2.0-84883739431 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13990 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84883739431&doi=10.1016%2fj.cclet.2013.06.019&partnerID=40&md5=232d167bb5e17de63b4966fa85cdd733 | |
dc.description.abstract | An operationally simple and eco-friendly protocol has been developed for the synthesis of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines 3 using the modified Pictet-Spengler reaction of N-sulfonylphenylethylamines 1 and various aldehydes 2 in the presence of tungstophosphoric acid hydrate. © 2013 Zhi-Jin Fan. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. | |
dc.title | Tungstophosphoric acid catalyzed synthesis of N-sulfonyl-1,2,3,4- tetrahydroisoquinoline analogs | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Chinese Chemical Letters. Vol 24, No.10 (2013), p.941-944 | |
dc.identifier.doi | 10.1016/j.cclet.2013.06.019 | |
Appears in Collections: | Scopus 1983-2021 |
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