134031-87-1Relevant academic research and scientific papers
5'-END DERIVATIVES
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, (2014/01/07)
The present invention provides compounds of formula (1). Another aspect of the invention relates to a method of inhibiting the expression of a gene in call, the method comprising (a) contacting an oligonucleotide of the invention with the cell; and (b) maintaining the cell from step (a) for a time sufficient to obtain degradation of the mRNA of the target gene.
Targeting chimeric α,β-oligonucleotides to the flanks of a stem in DNA. The enhanced effect of an intercalator
Khattab, Ahmed F.,Pedersen, Erik B.
, p. 1245 - 1252 (2007/10/03)
3′-O-(4,4′-Dimethoxytrityl)-5-methyl-N 4-(1-pyrenylmethyl)-α-cytidine (7) was prepared from α-thymidine by the reaction of 1-pyrenylmethylamine with an appropriate protected 4-(1,2,4-triazolyl)-α-thymidine derivative 5. 3′-O-(4,4′-Dimethoxytrit
Synthesis and physicochemical properties of alternating α,β-oligodeoxyribonucleotides with alternating (3' → 3')- and (5' → 5')-internucleotide phosphodiester linkages
Koga,Wilk,Moore,Scremin,Zhou,Beaucage
, p. 1520 - 1530 (2007/10/02)
A simple and straightforward synthesis of α-2'-deoxycytidine and α-2'-deoxyadenosine derivatives 6a,b has been achieved from commercial N4-benzoyl-b-2'-deoxycytidine and N6-benzoyl-β-2'deoxyadenosine, respectively. Properly protected
