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TRANS-THYMIDINE-CYCLIC-METHYL-3',5'-MONOPHOSPHATE
SpectraBase Compound ID JyC7CQN0czP
InChI InChI=1S/C11H15N2O7P/c1-6-4-13(11(15)12-10(6)14)9-3-7-8(19-9)5-18-21(16,17-2)20-7/h4,7-9H,3,5H2,1-2H3,(H,12,14,15)/i16+1
InChIKey PVZWVLPHVGPUIV-LOYIAQTISA-N
Mol Weight 319.22 g/mol
Molecular Formula C11H15N2O617OP
Exact Mass 319.065905 g/mol
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3CN
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3CN
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3CN
  • (R(P)-1)-THYMIDINE-CYCLIC-METHYL-3',5'-MONOPHOSPHATE
  • (S(P)-1)-THYMIDINE-CYCLIC-METHYL-3',5'-MONOPHOSPHATE
Title Journal or Book Year
17O NMR of diastereomeric 3′,5′-cyclic thymidine methyl phosphates, methylphosphonates, and N,N-dimethyl phosphoramidates. Phosphorus configuration of P-chiral [17O, 18O]-nucleoside phosphate diesters Tetrahedron Letters 1989
Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl-1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by water/iodine and oxygen/AIBN to P-chiral phosphates. Oxygen-17 NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates Journal of the American Chemical Society 1989

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