Nucleic Acids Research, 1977, Vol. 4, No. 8 2757-2765
© 1977
Articles |
A rapid and convenient synthesis of poly-thymidylic acid by the modified triester approach
Division of Biological Sciences, National Research Council of Canada Ottawa, KIA OR6 Canada
Received May 9, 1977.
By using anhydrous triethylamine-pyridine to selectively remove the cyanoethyl group from the fully protected oligo-nucleotide, a substantial improvement has been achieved in yields and the rates of condensation by the modified triester approach from the 5'
3' end. The unreacted oligonucleotide containing the 5'-hydroxy group was removed by treatment with bis (triazolyl)-p-chlorophenyl phosphate after each condensation in situ. These modifications, as exemplified by the synthesis of fully protected T12, T18, T24. and T38 in 80%, 77%, 70% and 50% yields respectively, should allow the ready synthesis of polynucleotides of even longer chain lengths by purely chemical methods.