A Robust Synthetic Route to 2‘-Deoxy-3‘-nucleotide Derivatives of Modified Nucleobases
Author:
Affiliation:
1. Department of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7400, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo982473i
Reference24 articles.
1. Two pyrene derivatives of widespread environmental distribution. Cyclopenta(cd)pyrene and acepyrene
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1. Synthesis and Absolute Configuration of Cis- and Trans-Opened Cyclopenta[cd]pyrene 3,4-Oxide N2-Deoxyguanosine Adducts: Conversion to Phosphoramidites for Oligonucleotide Synthesis;Chemical Research in Toxicology;2007-03-14
2. Palladium-Catalyzed Direct N-Arylation of Nucleosides, Nucleotides, and Oligonucleotides for Efficient Preparation of dG−N2 Adducts with Carcinogenic Amino-/Nitroarenes;The Journal of Organic Chemistry;2006-06-20
3. Identification of Stereochemical Configurations of Cyclopenta[ cd ]pyrene DNA Adducts in Strain A/J Mouse Lung and C3H10T1/2CL8 Cells;Polycyclic Aromatic Compounds;2002-01
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