AT Base Pair Anions versus (9-Methyl-A)(1-Methyl-T) Base Pair Anions-Reference-Cited by-同舟云学术

AT Base Pair Anions versus (9-Methyl-A)(1-Methyl-T) Base Pair Anions

Published:2005-04-08 Issue:17 Volume:127 Page:6443-6450
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Radisic Dunja¹,Bowen, Kit H.¹,Da̧bkowska Iwona¹,Storoniak Piotr¹,Rak Janusz¹,Gutowski Maciej¹

Affiliation:

1. Contribution from the Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, Department of Chemistry, University of Gdańsk, Sobieskiego 18, 80-952 Gdańsk, Poland, Institute of Organic Chemistry and Biochemistry, The Academy of Sciences of the Czech Republic (ASCR), Flemingovo nám.2, 166 10 Prague 6, Czech Republic, and Chemical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99352

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja050724g

Reference60 articles.

1. Global Minimum of the Adenine···Thymine Base Pair Corresponds Neither to Watson−Crick Nor to Hoogsteen Structures. Molecular Dynamic/Quenching/AMBER and ab Initio beyond Hartree−Fock Studies

2. True Stabilization Energies for the Optimal Planar Hydrogen-Bonded and Stacked Structures of Guanine···Cytosine, Adenine···Thymine, and Their 9- and 1-Methyl Derivatives: Complete Basis Set Calculations at the MP2 and CCSD(T) Levels and Comparison with Experiment

3. Properties of isolated DNA bases, base pairs and nucleosides examined by laser spectroscopy

4. Base pair analogs in the gas phase

5. Infrared depletion spectra of 2-aminopyridine⋅2-pyridone, a Watson–Crick mimic of adenine⋅uracil

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