N-ISOBUTYRYL-3'-O-LEVULINYL-2'-DEOXYGUANOSINE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 13CZInAAT4Q |
|---|---|
| InChI | InChI=1S/C19H25N5O7/c1-9(2)17(28)22-19-21-16-15(18(29)23-19)20-8-24(16)13-6-11(12(7-25)30-13)31-14(27)5-4-10(3)26/h8-9,11-13,25H,4-7H2,1-3H3,(H2,21,22,23,28,29)/t11-,12+,13+/m1/s1 |
| InChIKey | PSVAPVNSJMJAJV-AGIUHOORSA-N |
| Mol Weight | 435.44 g/mol |
| Molecular Formula | C19H25N5O7 |
| Exact Mass | 435.175398 g/mol |
| Enantiomer InChIKey | PSVAPVNSJMJAJV-YNEHKIRRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
deoxy-N-acetyl-2-amino-9.beta.- D-(diacetyl)ribofuranosyl)-9H-purine-6(1H)-one
3',5'-DI-O-LEVULINYL-2'-DEOXYGUANOSINE
3',5'-(TERT.-BUTYLDIMETHYLSILYLOXY)-2'-DEOXYGUANOSINE
2'-Deoxy-3',5'-bis-(tert-butyl-dimethylsilyl)-adenosine
2'-DEOXYGUANOSINE-3',5'-BIS-(ETHYL-HYDROGEN-PHOSPHATE)-2-DEOXY-2-HYDRO-RIBOFURANOSYL
3'-O-ACETYL-5'-O-DIMETHOXYTRITYL-2'-DEOXYINOSINE
YMADIINDONMITJ-BHDDXSALSA-N
[(2R,3R,4S,5R)-5-(2-AMINO-6-OXO-1,6-DIHYDROPURIN-9-YL)-3,4-DIHYDROXY-TETRAHYDROFURAN-2-YL]-METHYL-HYDROGEN-SULFATE
N-DIMETHYLAMINOETHYLENE-GUANOSINE
[(2S,3R,4S,5S)-5-(2-amino-6-keto-3H-purin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-trihydroxy-phosphonium
| Title | Journal or Book | Year |
|---|---|---|
| Building Blocks for the Solution Phase Synthesis of Oligonucleotides: Regioselective Hydrolysis of 3‘,5‘-Di-O-levulinylnucleosides Using an Enzymatic Approach | The Journal of Organic Chemistry | 2002 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.