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dc.contributor.authorRatchanok Pingaewen_US
dc.contributor.authorSupaluk Prachayasittikulen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.authorVirapong Prachayasittikulen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherCenter of Excellence on Environmental Healthen_US
dc.date.accessioned2018-10-19T04:47:01Z-
dc.date.available2018-10-19T04:47:01Z-
dc.date.issued2013-10-01en_US
dc.identifier.citationChinese Chemical Letters. Vol.24, No.10 (2013), 941-944en_US
dc.identifier.issn10018417en_US
dc.identifier.other2-s2.0-84883739431en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883739431&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/31511-
dc.description.abstractAn 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.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883739431&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleTungstophosphoric acid catalyzed synthesis of N-sulfonyl-1,2,3,4- tetrahydroisoquinoline analogsen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.cclet.2013.06.019en_US
Appears in Collections:Scopus 2011-2015

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