2015
DOI: 10.1016/j.tetlet.2015.03.072
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Synthesis of α-PNA containing a functionalized triazine as nucleobase analogue

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Cited by 2 publications
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“…The synthetic possibilities for the formation of alternative scaffolds bearing nitrogenous bases are virtually limitless. The development and study of hybridization properties of so-called peptide NAs built both on the classic aminoethyl glycine motif [169], as well as on the basis of dipeptide structures [170] and conformationally constrained analogs [171], has outgrown into a separate research area. In addition, combinations of the modifications described above allow one to obtain new types of oligonucleotides.…”
Section: Alternative Scaffolds For Nitrogenous Basesmentioning
confidence: 99%
“…The synthetic possibilities for the formation of alternative scaffolds bearing nitrogenous bases are virtually limitless. The development and study of hybridization properties of so-called peptide NAs built both on the classic aminoethyl glycine motif [169], as well as on the basis of dipeptide structures [170] and conformationally constrained analogs [171], has outgrown into a separate research area. In addition, combinations of the modifications described above allow one to obtain new types of oligonucleotides.…”
Section: Alternative Scaffolds For Nitrogenous Basesmentioning
confidence: 99%