Publication:
Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Simple item page
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.contributor.authorYodhathai Thebtaranonthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.date.accessioned2018-09-07T09:39:22Z
dc.date.available2018-09-07T09:39:22Z
dc.date.issued2001-07-30en_US
dc.description.abstractBoth forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts. © 2001 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Asymmetry. Vol.12, No.13 (2001), 1913-1922en_US
dc.identifier.doi10.1016/S0957-4166(01)00345-7en_US
dc.identifier.issn09574166en_US
dc.identifier.other2-s2.0-0035973760en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/26492
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035973760&origin=inwarden_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleSynthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactionsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035973760&origin=inwarden_US

Files

Collections

Scopus 2001-2005