A novel solid support for synthesis of oligonucleotide 3′-phosphorothioate monoesters

A new reagent immobilized on solid support allowing for solid-phase synthesis of oligonucleotides with a 3′-terminal phosphorothioate monoester is described. The support is compatible with phosphoramidite chemistry for automated oligonucleotide synthesis. Final deprotection with ammonia under standa...

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Bibliographic Details
Published inBioorganic & medicinal chemistry letters Vol. 13; no. 2; pp. 281 - 284
Main Authors Cheruvallath, Zacharia S, Cole, Douglas L, Ravikumar, Vasulinga T
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.01.2003
Elsevier
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Summary:A new reagent immobilized on solid support allowing for solid-phase synthesis of oligonucleotides with a 3′-terminal phosphorothioate monoester is described. The support is compatible with phosphoramidite chemistry for automated oligonucleotide synthesis. Final deprotection with ammonia under standard conditions leads to oligonucleotide 3′-terminal phosphorothioate. A new reagent immobilized on solid support allowing for solid-phase synthesis of oligonucleotides with a 3′-terminal phosphorothioate monoester is described. The support is compatible with phosphoramidite chemistry for automated oligonucleotide synthesis. Final deprotection with ammonia under standard conditions leads to oligonucleotide 3′-terminal phosphorothioate monoester (3′-TPT).
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ISSN:0960-894X
1464-3405
DOI:10.1016/S0960-894X(02)00922-8