Abstract
A synthetic route towards a selected set of N-acylated and N-alkylated derivatives of 2′-amino-α-L-LNA phosphoramidite building blocks has been developed. Biophysical studies suggest that the 2-oxo-5-azabicyclo[2.2.1] heptane skeleton of 2′-amino-α-L-LNA allows precise positioning of intercalators in the core of nucleic acid duplexes. Copyright © Taylor & Francis Group, LLC.
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Kumar, T. S., Madsen, A. S., Wengel, J., & Hrdlicka, P. J. (2007). Synthesis and biophysical studies of N2′-functionalized 2′-amino-α-L-LNA. Nucleosides, Nucleotides and Nucleic Acids, 26(10–12), 1403–1405. https://doi.org/10.1080/15257770701538841
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