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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 in:Bioorganic & medicinal chemistry letters 2003-01, Vol.13 (2), p.281-284
Main Authors: Cheruvallath, Zacharia S, Cole, Douglas L, Ravikumar, Vasulinga T
Format: Article
Language:English
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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).
ISSN:0960-894X
1464-3405
DOI:10.1016/S0960-894X(02)00922-8