Synthesis of a Phosphoramidite Coupling Unit of the Pyrimidine (6−4) Pyrimidone Photoproduct and Its Incorporation into Oligodeoxynucleotides
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (32), 7642-7643
- https://doi.org/10.1021/ja9603158
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Atomic model of a pyrimidine dimer excision repair enzyme complexed with a dna substrate: Structural basis for damaged DNA recognitionCell, 1995
- Mechanisms of DNA damage recognition in mammalian nucleotide excision repairThe FASEB Journal, 1995
- Endonuclease V from Bacteriophage T4 Interacts with Its Substrate in the Minor GrooveBiochemistry, 1994
- Accuracy of Replication Past the T-C (6-4) AdductJournal of Molecular Biology, 1994
- Labile exocyclic amine protection of nucleosides in DNA, RNA and oligonucleotide analog synthesis facililating N-deacylation, minimizing depurination and chain degradationBiochimie, 1993
- Repair by human cell extracts of single (6-4) and cyclobutane thymine-thymine photoproducts in DNA.Proceedings of the National Academy of Sciences of the United States of America, 1993
- The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli.Proceedings of the National Academy of Sciences of the United States of America, 1991
- Synthesis and characterization of a substrate for T4 endonuclease V containing a phosphorodithioate linkage at the thymine dimer siteNucleic Acids Research, 1990
- 3,4-Connected carbon nets: through-space and through-bond interactions in the solid stateJournal of the American Chemical Society, 1987