A1 Refereed original research article in a scientific journal

Oligonucleotides Incorporating Palladacyclic Nucleobase Surrogates




AuthorsMaity SK, Lonnberg T

PublisherWILEY-V C H VERLAG GMBH

Publication year2018

JournalChemistry - A European Journal

Journal name in sourceCHEMISTRY-A EUROPEAN JOURNAL

Journal acronymCHEM-EUR J

Volume24

Issue6

First page 1274

Last page1277

Number of pages4

ISSN0947-6539

DOIhttps://doi.org/10.1002/chem.201705797

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/30491162


Abstract
An oligonucleotide incorporating a palladacyclic nucleobase has been prepared by ligand-directed metalation of a phenylpyridine moiety. This oligonucleotide hybridized with natural counterparts placing any of the canonical nucleobases opposite to the palladacyclic residue. The palladated duplexes had B-type conformation and melting temperatures comparable to those of respective unmodified duplexes with a single mismatch. In the duplexes placing C, G or T (but not A) opposite to the palladacyclic residue, greatly increased absorptivity suggested formation of a Pd-II-mediated base pair. Absorptivity and ellipticity of these duplexes persisted even at the highest temperatures applicable in T-m and CD experiments (90 degrees C). Evidently the Pd-II-mediated base pairs do not dissociate under the experimental conditions.

Downloadable publication

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.





Last updated on 2024-26-11 at 15:08