A1 Refereed original research article in a scientific journal
Synthesis of Organometallic Oligonucleotides through Oximation with Metalated Benzaldehydes
Authors: Maity S.K., Lönnberg T.A.
Publisher: AMER CHEMICAL SOC
Publication year: 2019
Journal: ACS Omega
Journal name in source: ACS OMEGA
Journal acronym: ACS OMEGA
Volume: 4
Issue: 20
First page : 18803
Last page: 18808
Number of pages: 6
ISSN: 2470-1343
eISSN: 2470-1343
DOI: https://doi.org/10.1021/acsomega.9b02804
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/44064800
Abstract
A 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.
A 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.
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