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6-AMINO-9-(2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL)-PURINE
SpectraBase Compound ID LwO71eShpFq
InChI InChI=1S/C10H13N5O3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(17)6(2-16)18-7/h3-7,16-17H,1-2H2,(H2,11,12,13)/t5-,6+,7+/m0/s1
InChIKey OLXZPDWKRNYJJZ-RRKCRQDMSA-N
Mol Weight 251.25 g/mol
Molecular Formula C10H13N5O3
Exact Mass 251.101839 g/mol
Enantiomer InChIKey OLXZPDWKRNYJJZ-VQVTYTSYSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO;TFA=1EQ
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-17-1753-Fig2(c)
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 2'-deoxyadenosine
Title Journal or Book Year
Unambiguous structural elucidation of base-modified purine nucleosides using NMR Magnetic Resonance in Chemistry 2007
Complete1H and13C NMR spectral assignment of α- and β-adenosine, 2′-deoxyadenosine and their acetate derivatives Magnetic Resonance in Chemistry 2007
Water-Soluble Constituents of Fennel. IX. Glucides and Nucleosides. Chemical and Pharmaceutical Bulletin 1999
A sterol with an unusual side chain from Anoectochilus koshunensis Phytochemistry 1994
Base-Modified Nucleosides Related to 2-Chloro-2?-deoxyadenosine Helvetica Chimica Acta 1992
2?-Deoxyisoguanosine and Base-Modified Analogues: Chemical and Photochemical Synthesis Helvetica Chimica Acta 1991
Synthesis of 8-Aza-2?-deoxyadenosine and related 7-Amino-3H-1,2,3-triazolo[4,5-d]pyrimidine 2?-Deoxyribofuranosides: Stereoselective glycosylationvia the nucleobase anion Helvetica Chimica Acta 1989
The effect of protecting groups of the nucleobase and the sugar moieties on the acidic hydrolysis of the glycosidic bond of 2deoxyadenosine: a kinet Tetrahedron 1987

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