Deconvoluting the Reactivity of Two Intermediates Formed from Modified Pyrimidines-Reference-Cited by-同舟云学术

Deconvoluting the Reactivity of Two Intermediates Formed from Modified Pyrimidines

Published:2013-07-03 Issue:14 Volume:15 Page:3618-3621
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Weng Liwei¹,Horvat Sonia M.¹,Schiesser Carl H.¹,Greenberg Marc M.¹

Affiliation:

1. Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore Maryland 21218, United States, Australian Research Council Centre of Excellence for Free Radical Chemistry and Biotechnology, Australia, and School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Victoria, 3010, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401472m

Reference20 articles.

1. Photochemistry of phenyl thioethers and phenyl selenoethers. Radical vs. ionic behavior

2. Substituent Effects on the Photocleavage of Benzyl−Sulfur Bonds. Observation of the “Meta Effect”

3. PNA/DNA interstrand cross-links from a modified PNA base upon photolysis or oxidative conditions

4. 3′-Modified oligodeoxyribonucleotides for the study of 2-deoxyribose damage in DNA

5. Conformation, Lifetime, and Repair of 4‘-DNA Radicals

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