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dc.contributor.authorSakkarin Du-A-Manen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-09T02:06:12Z-
dc.date.available2018-11-09T02:06:12Z-
dc.date.issued2014-03-01en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2014, No.8 (2014), 1708-1715en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-84897628501en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84897628501&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/33628-
dc.description.abstractA synthesis of (+)-lentiginosine and its pyrrolizidine analogue was accomplished in six steps, starting from L-(+)-tartaric acid. The key step of these syntheses involves the intramolecular cyclization of α-sulfinyl carbanions for the construction of the indolizidine or pyrrolizidine ring. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84897628501&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleSynthesis of (+)-lentiginosine and its pyrrolizidine analogue based on intramolecular cyclization of α-sulfinyl carbanionsen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1002/ejoc.201301671en_US
Appears in Collections:Scopus 2011-2015

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