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Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59353
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dc.contributor.authorRattana Jongkolen_US
dc.contributor.authorRuangrat Choommongkolen_US
dc.contributor.authorBongkoch Tarnchompooen_US
dc.contributor.authorPiyarat Nimmanpipugen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.date.accessioned2018-09-10T03:14:12Z-
dc.date.available2018-09-10T03:14:12Z-
dc.date.issued2009-08-08en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-67649840195en_US
dc.identifier.other10.1016/j.tet.2009.06.016en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59353-
dc.description.abstractThe syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleSyntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonizationen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedronen_US
article.volume65en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsThailand National Center for Genetic Engineering and Biotechnologyen_US
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