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dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorJaray Panmuangen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-09T01:50:08Z-
dc.date.available2018-11-09T01:50:08Z-
dc.date.issued2014-10-14en_US
dc.identifier.citationTetrahedron. Vol.70, No.41 (2014), 7577-7583en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-84907059382en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907059382&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/33217-
dc.description.abstract© 2014 Elsevier Ltd. All rights reserved. A stereoselective approach to secolignans is described. The key synthetic strategy involves an asymmetric aldol reaction to control the creation of the stereogenic center at the β-carbon of the target secolignans. In the present work, peperomin C and its analogues, i.e., 2,6-didehydropeperomin C and 2-epi-peperomin C were successfully synthesized in good yields with high stereoselectivities.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907059382&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA stereoselective approach to bioactive secolignans: Synthesis of peperomin C and its analoguesen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.tet.2014.07.101en_US
Appears in Collections:Scopus 2011-2015

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