9(R)-[6(R)-hydroxymethyl-1-oxa-4-thiacyclohexan-2-yl]hypoxanthinen-water (4/3), a nucleoside analogue

Citation
G. Mazumder et al., 9(R)-[6(R)-hydroxymethyl-1-oxa-4-thiacyclohexan-2-yl]hypoxanthinen-water (4/3), a nucleoside analogue, ACT CRYST C, 57, 2001, pp. 560-561
Citations number
14
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS
ISSN journal
0108-2701 → ACNP
Volume
57
Year of publication
2001
Part
5
Pages
560 - 561
Database
ISI
SICI code
0108-2701(200105)57:<560:9(>2.0.ZU;2-0
Abstract
The title compound, 9(R)-[6(R)-hydroxymethyl-1-oxa-4-thiacyclohexan-2-yl]-1 ,9-dihydro-6H-purin-6-one-water (4/3), C10H12N4O3S .0.75H(2)O, crystallizes in the triclinic space group P1 with four molecules in the asymmetric unit and 0.75 waters of hydration per molecule. The structure was refined to an R value of 0.072 for 3382 observed reflections. The four crystallographica lly independent molecules are designated A, B, C and D. All four oxathiane rings adopt the chair conformation and the purine bases are in an anti orie ntation with respect to the sugar moieties. Molecules A and D and molecules C and B are base paired by a single hydrogen bond of the type N-H . . .N. These base pairs are again hydrogen bonded to their translated pairs in the direction of a cell diagonal.