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Palladium catalyzed allylation is under stereoelectronic control

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dc.contributor.authorRoderick W. Batesen_US
dc.contributor.authorPalangpon Kongsaereeen_US
dc.contributor.authorNunth Nontapattamadulen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.date.accessioned2018-09-07T09:39:30Z
dc.date.available2018-09-07T09:39:30Z
dc.date.issued2001-12-01en_US
dc.description.abstractPalladium catalyzed allylation of menthone and 4-t-butylcyclohexanone derivatives is shown to be under stereoelectronic control leading to the products of axial allylation. The stereochemical assignment is supported by1H NMR experiments and X-Ray crystallography of selected examples.en_US
dc.identifier.citationArkivoc. Vol.2001, No.1 (2001), 269-276en_US
dc.identifier.issn14246376en_US
dc.identifier.other2-s2.0-3042781293en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/26497
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=3042781293&origin=inwarden_US
dc.subjectChemistryen_US
dc.titlePalladium catalyzed allylation is under stereoelectronic controlen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=3042781293&origin=inwarden_US

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