Synthesis and biophysical studies of N2′-functionalized 2′-amino-α-L-LNA

4Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free