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Nucleic Acids Research, 1989, Vol. 17, No. 13 5291-5306
© 1989


MOLECULAR BIOLOGY

Pre–activation strategy for oligodeoxyribonudeotide synthesis using triaryloxydichloro–phosphoranes in the phosphotriester method

Hitoshi Hotoda, Takeshi Wada, Mitsuo Sekine and Tsujiaki Hata*

Department of Life Chemistry, Tokyo Institute of Technology Nagatsuta, Midoriku, Yokohama 227, Japan

*To whom correspondence should be addressed

Received March 22, 1989. Revised May 30, 1989. Accepted May 30, 1989.

Triaryloxydlchlorophosphoranes were tested as condensing agents for Oliodeoxyribonudeotide synthesis in the phosphotriester method. Tris(2,4,6–tribromophenoxy)dlchlorophosphorane (BDCP) was found to be a relatively stable crystalline material which could be used as a chemical reagent. A notable feature of the BDCP-promoted condensation reaction was studied by a small amount of BDCP compared to the conventional condensing agent was effective for the generation of active nucleotide intermediates and BDCP itself was quantitatively converted into an inert material, tris(2,4,6-tribromophenyl)phosphate (2)– Thus, BDCP enabled us to separate the activation step from the condensation process in the phosphotriesterm ethod. This preactivation method was applied to the solid-phase synthesis.


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