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Guanosine
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
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Solvent DMSO-D6
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 and 15N,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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