2014
DOI: 10.1016/j.bmcl.2014.06.027
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Synthesis of 3′-triazoyl-dinucleotides as precursors of stable Phe-tRNAPhe and Leu-tRNALeu analogues

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Cited by 2 publications
(1 citation statement)
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“…and co-workers). These include oxadiazole and triazole linkages, mimicking esters in the 3′ or 2′ position of the 3′-terminal ribose of the aminoacyl-tRNA. The oxadiazole can be introduced into the 3′-position of adenosine, and the corresponding RNA can be obtained following a chemical-enzymatic approach using classical phosphoramidite chemistry to produce the 3′-modified dinucleotides followed by enzymatic ligation using T4 RNA ligase (Figure A).…”
Section: Heterocyclic- and Squarate-linked Peptidyl-trna Mimicsmentioning
confidence: 99%
“…and co-workers). These include oxadiazole and triazole linkages, mimicking esters in the 3′ or 2′ position of the 3′-terminal ribose of the aminoacyl-tRNA. The oxadiazole can be introduced into the 3′-position of adenosine, and the corresponding RNA can be obtained following a chemical-enzymatic approach using classical phosphoramidite chemistry to produce the 3′-modified dinucleotides followed by enzymatic ligation using T4 RNA ligase (Figure A).…”
Section: Heterocyclic- and Squarate-linked Peptidyl-trna Mimicsmentioning
confidence: 99%