Oligonucleotide synthesis using the 2-(levulinyloxymethyl)-5-nitrobenzoyl group for the 5 '-position of nucleoside 3 '-phosphoramidite derivatives

A comparative study on the utility of 2-(levulinyloxymethyl)-5-nitrobenzoyl (LMNBz) and 2-(levulinyloxymethyl)benzoyl (LMBz) protecting groups for the 5'-positions of nucleoside 3'-phosphoramidite derivatives in the oligonucl eotide synthesis is presented in terms of the syntheses of TpTpT, TpTpTpT, and UpCpApGpUpUpGpG. In addition we describe the synthesis, using the LMNBz protecting group of the CpCpA terminus triplet of tRNAs bearing exocyclic amino groups with N-15-labeling, and the trimer Gp[A*]pG containing 2'-O-(b eta-D-ribofuranosyl)adenosine ([A*]), the latter of which is found at posit ion 64 in the yeast initiator tRNA(Met).