Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes

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dc.contributor.authorMaity S.K.
dc.contributor.authorLönnberg T.A.
dc.contributor.organizationfi=lääkekehityksen kemia|en=Pharmaseutical Chemistry|
dc.contributor.organization-code1.2.246.10.2458963.20.93793350823
dc.contributor.organization-code2606303
dc.converis.publication-id44064800
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/44064800
dc.date.accessioned2022-10-28T13:57:13Z
dc.date.available2022-10-28T13:57:13Z
dc.description.abstractA phthaloyl-protected aminooxymethyl-C-2'-deoxyriboside building block has been prepared and incorporated in the middle of an oligodeoxyribonucleotide. Removal of the phthaloyl protection followed by on-support oximation with either mercurated or palladated benzaldehydes yielded oligonucleotides bearing the respective benzaldoxime metallacycles.
dc.format.pagerange18803
dc.format.pagerange18808
dc.identifier.eissn2470-1343
dc.identifier.jour-issn2470-1343
dc.identifier.olddbid185398
dc.identifier.oldhandle10024/168492
dc.identifier.urihttps://www.utupub.fi/handle/11111/42185
dc.identifier.urnURN:NBN:fi-fe2021042824429
dc.language.isoen
dc.okm.affiliatedauthorMaity, Sajal
dc.okm.affiliatedauthorLönnberg, Tuomas
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAMER CHEMICAL SOC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1021/acsomega.9b02804
dc.relation.ispartofjournalACS Omega
dc.relation.issue20
dc.relation.volume4
dc.source.identifierhttps://www.utupub.fi/handle/10024/168492
dc.titleSynthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes
dc.year.issued2019

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