@article{33b6bbf8c4324a4bbbea836073e7be96,
title = "13C-NMR of ribosyl A-A-A, A-A-G, AND A-U-G Synthesis and Assignment",
abstract = "The three RNA trinucleotides; ApApA, ApApG, and ApUpG, have been synthesized in sufficient quantity to obtain natural abundance 13C{1H}-NMR spectra at strand concentrations between 4 and 100 mM. Comparisons between 70°C spectra of the three trimers and their consistuent dimers ApA, ApG, ApU, and UpG allow secure assignments to be made for most of the resonances. This paper describes the syntheses and 13C assignments of the oligomers.",
keywords = "C - NMR, Comparative assignment, Trinucleotide",
author = "Stone, {Michael P.} and Winkle, {Stephen A.} and McFarland, {Gloria D.} and Yoo, {Min C.} and Borer, {Philip N.}",
note = "Funding Information: We thank C. Moore (U.C. Irvine), J. Dallas and J. Matson (U.C. Davis) for assistancei n obtaining some of the spectra. This work was supported by the National Institutes of Health (grants GM24494 and GM32691 to P.N.B.), instrument grants from the National Science Foundation (CHE-79-10821 to U.C. Irvine and CHE-79-04832 to U.C. Davis), and NIH grant RR01317 for the NIH Research Resource for Multi-Nuclei NMR and Data Processing at Syracuse University (to G. Levy and P.N.B.).",
year = "1985",
month = nov,
doi = "10.1016/0301-4622(85)80071-5",
language = "English (US)",
volume = "23",
pages = "129--138",
journal = "Biophysical Chemistry",
issn = "0301-4622",
publisher = "Elsevier",
number = "1-2",
}