Replacement of the Phosphodiester Backbone of Oligodeoxynucleotide Analogues by Non-Ionic Phosphoramidate (P-NH2)
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[1] B. Rayner,et al. Dramatic effect of the anomeric configuration on the thermal stability of duplex formed between novel dodecathymidine phosphoramidate (PNH2) and complementary DNA and RNA strands , 1996 .
[2] B. Rayner,et al. Oligodeoxynucleoside phosphoramidates (P-NH2): synthesis and thermal stability of duplexes with DNA and RNA targets. , 1996, Nucleic acids research.
[3] N. Ho,et al. N-pent-4-enoyl nucleosides: Application in the synthesis of support-bound and free oligonucleotide analogs by the H-phosphonate approach , 1996 .
[4] R. Varma. Synthesis of Oligonucleotide Analogues with Modified Backbones , 1994 .
[5] J. C. Martin,et al. Current concepts in antisense drug design. , 1993, Journal of medicinal chemistry.
[6] B. Froehler,et al. Phosphoramidate analogues of DNA: synthesis and thermal stability of heteroduplexes. , 1988, Nucleic acids research.
[7] R. Letsinger,et al. Effects of pendant groups at phosphorus on binding properties of d-ApA analogues. , 1986, Nucleic acids research.
[8] B. Froehler. Deoxynucleoside H-Phosphonate diester intermediates in the synthesis of internucleotide phosphate analogues , 1986 .