SpectraBase Compound ID | 2yC0a2F9ixX |
---|---|
InChI | InChI=1S/C10H13N5O5/c11-10-13-7-4(8(19)14-10)12-2-15(7)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m0/s1 |
InChIKey | NYHBQMYGNKIUIF-GIMIYPNGSA-N |
Mol Weight | 283.24 g/mol |
Molecular Formula | C10H13N5O5 |
Exact Mass | 283.091669 g/mol |
Enantiomer InChIKey | NYHBQMYGNKIUIF-UUOKFMHZSA-N |
Title | Journal or Book | Year |
---|---|---|
Oligodeoxyribonucleotide Analogues with Bridging Dimethylene Sulfide, Sulfoxide, and Sulfone Groups. Toward a Second-Generation Model of Nucleic Acid Structure | The Journal of Organic Chemistry | 2002 |
Nucleosides and Nucleotides. 184. Synthesis and Conformational Investigation of Anti-Fixed 3-Deaza-3-halopurine Ribonucleosides1,2 | The Journal of Organic Chemistry | 1999 |
Synthesis and Properties of N-Phosphorylated Ribonucleosides | Journal of the American Chemical Society | 1994 |
15N NMR spectra of wyosine (Y-nucleoside) triacetate and its 7-methyl congener. Chemical shifts and15N,1H coupling constants | Magnetic Resonance in Chemistry | 1988 |
An 15n-nmr study of isomeric n1 and n3 substituted 7-methyl-10-oxo-9,10-dihydro pyrimido[l,2-a]purines and 9-oxo-8,9-dihydro-5-alkyl-imidazo[1,2-a] purines in neutral and acidic medium. | Tetrahedron | 1987 |
An assessment of the reactivity of guanosine and some of its derivatives to electrophiles by 15N-NMR spectroscopy | Tetrahedron | 1986 |
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