Abstract
The catching-by-polymerization (CBP) oligodeoxynucleotide (oligo or ODN) purification method has been demonstrated suitable for large-scale, parallel, and long oligo purification. The authenticity of the oligos has been verified via DNA sequencing. Gene construction and expression have been demonstrated. A remaining obstacle to the practical utility of the CBP method is affordable polymerizable tagging phosphoramidites (PTPs) that are needed for the method. In this article, we report scalable synthesis of the four nucleoside (dA, dC, dG and dT) precursors to the PTPs using a route having six steps from inexpensive starting materials. The overall yields ranged from 21% to 35%. The scales of the synthesis presented here are up to 2.1 grams of the precursors. Because the syntheses are chromatography-free, they are predicted to be readily scalable. With the precursors, the PTPs can be synthesized in one step using standard methods involving a chromatography purification.
Supplementary materials
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Supporting Information
Description
Images of compound, TLC, and 1H and 13C NMR spectra for compounds 6-9 and 10a-d, and MS of compounds 10a-d
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