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. 1992 Jan-Feb;3(1):85-7.
doi: 10.1021/bc00013a014.

An improved CPG support for the synthesis of 3'-amine-tailed oligonucleotides

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An improved CPG support for the synthesis of 3'-amine-tailed oligonucleotides

C R Petrie et al. Bioconjug Chem. 1992 Jan-Feb.

Abstract

A new controlled-pore glass (CPG) support is described that allows for the direct synthesis of oligonucleotides bearing a 3'-aminohexyl tail. This solid support (AH-CPG) exhibits superior performance as compared to a commercially available 3'-amine CPG. The AH-CPG is prepared from 6-aminohexan-1-ol with a unique protecting group for the amine that also functions as the site of attachment to the CPG. A 3'-amine-tailed oligodeoxynucleotide (ODN) was prepared from this support using standard phosphoramidite coupling and deprotection conditions. The 3'-amine-tailed ODN was subsequently modified with an acridinylpropionic acid tetrafluorophenyl ester. Facile synthesis of the AH-CPG and the stability of the deprotected product makes this functionalized solid support especially useful for preparation of oligonucleotides bearing 3'-amine tails and other modifications.

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