Base-Pairing Energies of Proton-Bound Dimers and Proton Affinities of 1-Methyl-5-Halocytosines: Implications for the Effects of Halogenation on the Stability of the DNA i-Motif
Author:
Affiliation:
1. Department of Chemistry, Wayne State University, 48202, Detroit, MI, USA
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
http://link.springer.com/content/pdf/10.1007/s13361-015-1174-2.pdf
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2. Influence of 2′-Modifications (O-Methylation, Fluorination, and Stereochemical Inversion) on the Base Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities ofi-Motif Structures;Journal of the American Society for Mass Spectrometry;2023-06-09
3. A Comprehensive Ab Initio Study of Halogenated A···U and G···C Base Pair Geometries and Energies;International Journal of Molecular Sciences;2023-03-14
4. Influence of 5-Halogenation on the Base-Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities of Synthetic i-Motif Structures for DNA Nanotechnology Applications;Journal of the American Society for Mass Spectrometry;2022-08-03
5. Influence of 5-Methylation and the 2′- and 3′-Hydroxy Substituents on the Base Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities of i-Motif Structures;The Journal of Physical Chemistry A;2021-07-06
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