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Base Modification and the Phosphoramidite Approach

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Pages 297-300 | Published online: 05 Dec 2006

References

  • Beaucage , S. L. and Caruthers , M. H. 1981 . Tetrahedron Lett. , 22 : 1859 – 1862 .
  • Adams , S. P. , Kavka , K. S. , Wykes , E. , Holder , S. B. and Galluppi , G. R. 1983 . J. Am. Chem. Soc. , 105 : 661
  • Efcavitch , J. W. 2nd International Symposium on Phosphorous Chemistry Directed Towards Biology . Poland
  • McBride , L. J. , Kierzek , R. , Beaucage , S. L. and Caruthers , M. H. 1986 . J. Am. Chem. Soc , 108 : 2040 – 2048 .
  • Pon , R. T. , Damha , M. J. and Ogilvie , K. K. 1985 . Tetrahedron Lett. , 26 : 2525 – 2528 .
  • Gau , X. , Gaffney , B. L. , Senior , M. , Riddle , R. R. and Jones , R. A. 1985 . Nucleic Acids Res., JJ , : 573 – 584 .
  • Urdea , M. S. , Ku , L. , Horn , T. , Gee , Y. G. and Warner , B. D. 1985 . Nucleic Acids Res. , 16 : 257 – 260 .
  • All oligomers were synthesized at 0.2 umol scale on an Applied Bio‐systems 381A DNA Synthesizer with the same set of reagents all commercially available from Applied Biosystems (ABI) as of 9/1/86, with the exception that the 150‐mers were synthesized on a “wide pore” CPG support (1000A0, 18 umol/g deoxycytidine). Cycle‐2 (ABI User Bulletin No. 6, Revised 7/1/86) and Cycle‐1 (ABI User Bulletin No. 1, 11/1/85), were used for “2‐cyanoethyl” and “methyl” syntheses, respectively. Deprotections were performed manually: 1) Thiophenoxide solution (0.5 h, 25°C, methyl syntheses only) followed by cone NH, (aq) (53°C, 10–16h).
  • Cathcart , R. 3Manuscript in preparation

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