Aromaticity of nucleic acid bases-Reference-Cited by-同舟云学术

Aromaticity of nucleic acid bases

Published:2020-12-13 Issue:4 Volume:11 Page:
ISSN:1759-0876
Container-title:WIREs Computational Molecular Science
language:en
Short-container-title:WIREs Comput Mol Sci

Author:

Szatylowicz Halina¹^ORCID,Stasyuk Olga A.²^ORCID,Solà Miquel²^ORCID,Krygowski Tadeusz M.³^ORCID

Affiliation:

1. Faculty of Chemistry Warsaw University of Technology, Noakowskiego 3, 00‐664 Warsaw Poland

2. Institute of Computational Chemistry and Catalysis and Department of Chemistry, University of Girona, C/ Maria Aurélia Capmany 69, 17003 Girona Spain

3. Faculty of Chemistry Warsaw University, Pasteura 1, 02‐093 Warsaw Poland

Funder

Generalitat de Catalunya

Ministerio de Economía y Competitividad

Narodowe Centrum Nauki

Publisher

Wiley

Subject

Materials Chemistry,Computational Mathematics,Physical and Theoretical Chemistry,Computer Science Applications,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/wcms.1509

Reference109 articles.

1. Hydrogen bond design principles

2. Introduction: Aromaticity

3. Introduction: DelocalizationPi and Sigma

4. Tautomerism in nucleic acid bases and base pairs: a brief overview

5. Connecting and combining rules of aromaticity. Towards a unified theory of aromaticity

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ultrasensitive detection of trace Hg(Ⅱ) in acidic conditions using DMABR loaded on sepiolite: Function, application and mechanism studies;Journal of Hazardous Materials;2024-08

2. DNA as a perfect quantum computer based on the quantum physics principles;Scientific Reports;2024-05-21

3. Biomimetic nucleotide-graphene hybrids for electrocatalytic oxygen conversion: Quantifying biomolecule mass loading;Sustainable Materials and Technologies;2024-04

4. Insights into the Ozonation of Antiviral Purine Derivatives by the Basic Structures’ Kinetics and Ozone Consumption Ratios;ACS ES&T Water;2023-05-12

5. Synthesis, characterization, crystal structure, and fluorescence behavior of new 4-aryl-6-(2,5-dichlorothiophen-3-yl)-2-methylpyridine-3-carbonitrile derivatives;Journal of Molecular Structure;2023-01