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Original Articles

SILYL PROTECTING GROUPS FOR OLIGONUCLEOTIDE SYNTHESIS REMOVED BY A ZnBr2 TREATMENT

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Pages 1009-1013 | Published online: 15 Nov 2011

REFERENCES

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  • Shute , R. E. and Rich , D. H. 1987 . Synthesis and evaluation of novel activated mixed carbonate reagents for the introduction of the 2-(trimethylsilyl)ethoxycarbonyl(Teoc)-protecting group . Synthesis , : 346 – 349 .
  • Waldmann , H. , Reidel , A. , Heuser , A. , Muhlegger , K. , Von der Eltz , H. and Birkner , C. 1994 . Verwendung von mit enzymatisch abspaltbaren schutzgruppen versehenen nukleosiden und nukleosid-derivaten in der synthese von oligonukleotiden EP 0 649 855 A1
  • Kataoka , M. , Hattori , A. , Okino , S. , Hyodo , M. , Asano , M. R.K. and Hayakawa , Y. 2001 . Ethyl(methyl)dioxirane as an efficient reagent for the oxidation of nucleoside phosphites into phosphates under nonbasic anhydrous conditions . Org. Lett. , 3 : 815 – 818 .
  • Thuong , N. T. and Asseline , U. 1991 . “ Oligonucleotides attached to intercalators, photoreactive and cleavage agents ” . In Oligonucleotides and Analogues. A Practical Approach , 283 – 308 . Oxford : Oxford University Press .

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