A simple solid-phase procedure allows cyclic oligoribonucleotides to be obtained as long as the linear precursor attached to the support has a 2′-deoxyribonucleoside or a 2′-O-methylribonucleoside at the 3′-end.
M. Frieden, A. Grandas and E. Pedroso, Chem. Commun., 1999, 1593 DOI: 10.1039/A904851K
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