Synthesis of fully protected trinucleotide building blocks on a disulphide-linked soluble support

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dc.contributor.authorSuchsland Ruth
dc.contributor.authorAppel Bettina
dc.contributor.authorVirta Pasi
dc.contributor.authorMüller Sabine
dc.contributor.organizationfi=lääkekehityksen kemia|en=Pharmaseutical Chemistry|
dc.contributor.organization-code1.2.246.10.2458963.20.93793350823
dc.converis.publication-id53410037
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/53410037
dc.date.accessioned2022-10-28T14:32:01Z
dc.date.available2022-10-28T14:32:01Z
dc.description.abstractIn recent years, preparation of fully protected trinucleotide phosphoramidites as synthons for the codon-based synthesis of gene libraries as well as for the assembly of oligonucleotides from blockmers has gained much attention. We here describe the preparation of such trinucleotide synthons on a soluble support using a disulphide linker.
dc.format.pagerange3892
dc.format.pagerange3896
dc.identifier.eissn2046-2069
dc.identifier.olddbid188821
dc.identifier.oldhandle10024/171915
dc.identifier.urihttps://www.utupub.fi/handle/11111/56197
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2021/RA/D0RA10941J#!divAbstract
dc.identifier.urnURN:NBN:fi-fe2021042826969
dc.language.isoen
dc.okm.affiliatedauthorVirta, Pasi
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherROYAL SOC CHEMISTRY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1039/d0ra10941j
dc.relation.ispartofjournalRSC Advances
dc.relation.issue7
dc.relation.volume11
dc.source.identifierhttps://www.utupub.fi/handle/10024/171915
dc.titleSynthesis of fully protected trinucleotide building blocks on a disulphide-linked soluble support
dc.year.issued2021

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