Abstract
Synthesis of xylo-LNA containing one 2'-O,4'-C-methylene-β-D-xyrofuranosyl thymine nucleotide monomer and α-L-LNAs containing one or four 2'-O,4'-C-methylene-α-L-ribofuranosyl thymine nucleotide monomer(s) has been accomplished using phosphoramidite chemistry with pyridine hydrochloride as activator; oligothymidylate α-L-LNA displays strongly enhanced affinity towards complementary RNA.
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CITATION STYLE
Rajwanshi, V. K., Håkansson, A. E., Dahl, B. M., & Wengel, J. (1999). LNA stereoisomers: Xylo-LNA (B-D-xylo configured locked nucleic acid) and α-L-LNA (α-L-ribo configured locked nucleic acid). Chemical Communications, (15), 1395–1396. https://doi.org/10.1039/a903189h
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