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Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1H-Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium Hexafluorophosphate

Two approaches for C4 modifications of silyl-protected thymidine, 2′-deoxyuridine, and 3′-azido-2′,3′-dideoxythymidine (AZT) are described. In both, nucleoside amide activation with 1H-benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and DBU yields O(4)-(benzotriazol-1-y...

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書誌詳細
出版年:Curr Protoc Nucleic Acid Chem
主要な著者: Akula, Hari K., Lakshman, Mahesh K.
フォーマット: Artigo
言語:Inglês
出版事項: 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6834435/
https://ncbi.nlm.nih.gov/pubmed/30688408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cpnc.73
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