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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

Ashwani K. Sood and Saran A. Narang

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.


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