Roivainen, Jarkko, Reuter, Hans, Mikhailopulo, Igor A., Eickmeier, Henning (2007) Methyl 1-deoxy-1-(N 1-thyminyl)-β-D-psicofuranoside. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807048866
| Reference Type | Journal (article/letter/editorial) | ||
|---|---|---|---|
| Title | Methyl 1-deoxy-1-(N 1-thyminyl)-β-D-psicofuranoside | ||
| Journal | Acta Crystallographica Section E Structure Reports Online | ||
| Authors | Roivainen, Jarkko | Author | |
| Reuter, Hans | Author | ||
| Mikhailopulo, Igor A. | Author | ||
| Eickmeier, Henning | Author | ||
| Year | 2007 (November 1) | Volume | 63 |
| Issue | 11 | ||
| Publisher | International Union of Crystallography (IUCr) | ||
| DOI | doi:10.1107/s1600536807048866Search in ResearchGate | ||
| Generate Citation Formats | |||
| Mindat Ref. ID | 466994 | Long-form Identifier | mindat:1:5:466994:8 |
| GUID | 0 | ||
| Full Reference | Roivainen, Jarkko, Reuter, Hans, Mikhailopulo, Igor A., Eickmeier, Henning (2007) Methyl 1-deoxy-1-(N 1-thyminyl)-β-D-psicofuranoside. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807048866 | ||
| Plain Text | Roivainen, Jarkko, Reuter, Hans, Mikhailopulo, Igor A., Eickmeier, Henning (2007) Methyl 1-deoxy-1-(N 1-thyminyl)-β-D-psicofuranoside. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807048866 | ||
| In | (2007, November) Acta Crystallographica Section E Structure Reports Online Vol. 63 (11) International Union of Crystallography (IUCr) | ||
| Abstract/Notes | In the structure of the title compound, C12H18N2O7, the furanosyl ring adopts the S-type sugar pucker with the following pseudorotational parameters: PS = 159.6° (C2′-endo according to the designation of the ribofuranose ring of natural nucleosides; C3′-endo according to the numbering of the title compound) and νmax = 35.9°. The conformation around the C5′—C6′ bond is ap (gauche–trans; gt; −g), with a torsion angle γ of −170.3 (2)°. The structure of the thymine base is very similar to that of thymidine. There are intermolecular N—H...O and O—H...O hydrogen bonds. | ||
See Also
These are possibly similar items as determined by title/reference text matching only.
