Abstract
A short synthetic route to the first β-l-ribo configured locked nucleic acid (LNA), that is, 2′-amino-β-l-LNA thymine phosphoramidite 6, has been developed from bicyclic nucleoside 1. Incorporation of 2′-amino-β-l-LNA thymine monomers into α-DNA strands results in probes forming stable duplexes with complementary RNA in parallel orientation. © 2009 Elsevier Ltd. All rights reserved.
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Kumar, T. S., Østergaard, M. E., Sharma, P. K., Nielsen, P., Wengel, J., & Hrdlicka, P. J. (2009). Parallel RNA-strand recognition by 2′-amino-β-l-LNA. Bioorganic and Medicinal Chemistry Letters, 19(9), 2396–2399. https://doi.org/10.1016/j.bmcl.2009.03.079
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