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- W2012798371 abstract "Cyanoethyl-protected phosphotriester links in oligonucleotides made with standard pophosporamidite chemistry were converted to pbosphoramidate linkages during oligonucleotide synthesis on solid support. The cyanoethyl group was removed with piperidine, and the resulting phosphodiester was activated with p-tosyl chloride. An amine nucleophile displaced the tosyl to yield a phosphoramidate linkage." @default.
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- W2012798371 modified "2023-09-27" @default.
- W2012798371 title "A new method for introducing amidate linkages in oligonucleotides using phosphoramidite chemistry" @default.
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- W2012798371 doi "https://doi.org/10.1016/s0960-894x(99)00467-9" @default.
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