NMR studies of nucleic acids. Deuterium isotope effects on carbon-13 chemical shifts in hydrogen-bonded complexes of pyrimidines and purines
- 1 November 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 110 (23) , 7640-7647
- https://doi.org/10.1021/ja00231a010
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Protonated base pairs explain the ambiguous pairing properties of O6-methylguanine.Proceedings of the National Academy of Sciences, 1987
- Nonempirical calculations on all the 29 possible DNA base pairsJournal of the American Chemical Society, 1987
- Isotopic multiplets in the carbon-13 NMR spectra of aniline derivatives and nucleosides with partially deuterated amino groups: effect of intra- and intermolecular hydrogen bondingJournal of the American Chemical Society, 1987
- Intramolecular hydrogen bonding as reflected in the deuterium isotope effects on carbon-13 chemical shifts. Correlation with hydrogen bond energiesJournal of the American Chemical Society, 1986
- Hydrogen bonding and biological specificity analysed by protein engineeringNature, 1985
- Nuclear Overhauser effect in specifically deuterated macromolecules: NMR assay for unusual base pairing in transfer RNA.Proceedings of the National Academy of Sciences, 1980
- The synthesis of oligoribonucleotides. III. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VIIICanadian Journal of Chemistry, 1979
- 2',3',5'-Tri-O-benzoyl[4-13C]uridine. An efficient, regiospecific synthesis of the pyrimidine ringThe Journal of Organic Chemistry, 1978
- Detection of proton acceptor sites of hydrogen bonding between nucleic acid bases by the use of carbon-13 magnetic resonanceJournal of the American Chemical Society, 1977
- Association by hydrogen bonding of free nucleosides in non-aqueous solutionJournal of Molecular Biology, 1966