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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Published in | Bioorganic & medicinal chemistry letters Vol. 13; no. 2; pp. 281 - 284 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier Ltd
01.01.2003
Elsevier |
Subjects | |
Online Access | Get full text |
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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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/S0960-894X(02)00922-8 |