Issue 11, 1980

Synthesis of 4-nitrophenyl esters of thymidine 3′-phosphate and 3′-phosphorothioate using a new phosphorylating agent

Abstract

2′-Deoxynucleoside-3′-O-(4-nitrophenyl) phosphoranilidates (e.g., 2), prepared by the action of O-(4-nitrophenyl)N-phenylphosporamidochloridate (1) on alcohols, are converted into the corresponding 4-nitrophenyl phosphate esters (e.g., 3) or P-chiral 4-nitrophenyl phosphorothioate esters (e.g., 4) by treatment with NaH–CX2(X = O or S).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 524-525

Synthesis of 4-nitrophenyl esters of thymidine 3′-phosphate and 3′-phosphorothioate using a new phosphorylating agent

W. Niewiarowski, W. J. Stec and W. S. Zielinski, J. Chem. Soc., Chem. Commun., 1980, 524 DOI: 10.1039/C39800000524

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