Nucleic Acid Oxidation Mediated by Naphthalene and Benzophenone Imide and Diimide Derivatives: Consequences for DNA Redox Chemistry-Reference-Cited by-同舟云学术

Nucleic Acid Oxidation Mediated by Naphthalene and Benzophenone Imide and Diimide Derivatives: Consequences for DNA Redox Chemistry

Published:1999-04-01 Issue:16 Volume:121 Page:3854-3861
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rogers Joy E.¹,Kelly Lisa A.¹

Affiliation:

1. Contribution from the Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9841299

Reference30 articles.

1. Photocleavage of Nucleic Acids

2. Photochemical Mechanisms Responsible for the Versatile Application of Naphthalimides and Naphthaldiimides in Biological Systems

3. Bis(hydroperoxy)naphthaldiimide as a“Photo-Fenton Reagent”: Sequence-Specific Photocleavage of DNA

4. Photoinduced DNA Cleavage via Electron Transfer: Demonstration That Guanine Residues Located 5' to Guanine Are the Most Electron-Donating Sites

5. Photoactivatable DNA-Cleaving Amino Acids: Highly Sequence-Selective DNA Photocleavage by Novel L-Lysine Derivatives

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