Abstract
Adenylyl(3''-5'')adenosine cyclic 2'',3''-phosphate (A-A > p) was synthesized and its polymerization was attempted under various conditions in the presence of poly(U) and 1,3-propanediamine. Reaction at -20.degree. C for 16 days gave polymerized products (up to the 8-mer) in 15% yield and was proved to be dependent on the template. Reaction at 0.degree. C for 16 days gave more extensive (up to the 10-mer) and more efficient (35%) polymerization. The newly formed phosphodiester linkage was exclusively 2''-5''. These results are discussed in comparison with the monomer-condensation reaction.

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