Tungstophosphoric acid catalyzed synthesis of N-sulfonyl-1,2,3,4- tetrahydroisoquinoline analogs

Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13990

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DC Field	Value	Language
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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