Artificial Genetic Systems: Exploiting the “Aromaticity” Formalism To Improve the Tautomeric Ratio for Isoguanosine Derivatives
Author:
Affiliation:
1. Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611-7200 benner@chem.ufl.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0497959
Reference43 articles.
1. Nucleobase Pairing in Expanded Watson-Crick-like Genetic Information Systems
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3. PCR amplification of DNA containing non-standard base pairs by variants of reverse transcriptase from Human Immunodeficiency Virus-1
4. Tautomerism of Isoguanosine and Solvent-Induced Keto-Enol Equilibrium
5. 2‘-Deoxyisoguanosine Adopts More than One Tautomer To Form Base Pairs with Thymidine Observed by High-Resolution Crystal Structure Analysis
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3. DNA with Purine–Purine Base Pairs: Size and Position of Isoguanine and 8-Aza-7-deazaisoguanine Clickable Residues Control the Molecular Recognition of Guanine and 5-Aza-7-deazaguanine;The Journal of Organic Chemistry;2022-08-10
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