The ring itself has a boat conformation. C-HÁ Á ÁO interactions link the molecules into a chain in the [010] direction.
(3S,6R)-3-Benzyloxymethyl-6-methyl-1,4-dioxane-2,5-dione
✍ Scribed by Kooijman, Huub ;Leemhuis, Mark ;Nostrum, Cornelus F. van ;Hennink, Wim E. ;Spek, Anthony L.
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 193 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
The ring itself has a somewhat flattened twist-boat conformation. C-HÁ Á ÁO interactions join the molecules into a twodimensional network running parallel to the (101) plane.
📜 SIMILAR VOLUMES
The lactide ring in the title compound, C 12 H 12 O 5 , adopts a screw-boat conformation. C-HÁ Á ÁO interactions link the molecules into a chain in the [100] direction.
This work describes the first solid-state structural study of a cyclic enaminone derivative from Meldrum's acid, C 10 H 13 NO 4 . The packing shows an infinite linear chain along [111] mediated by dimeric N-HÁ Á ÁO and nonclassical C-HÁ Á ÁO hydrogen-bonding interactions.
The crystal structure of the title compound, C 23 H 28 Br 4 O 6 , confirms that it consists of two hexasubstituted aromatic units linked by a central methylene group. The molecule lies on a crystallographic twofold axis that passes through the methylene bridging atom. Examination of the extended str
In the title compound, C 12 H 13 NO 3 , the angles at the Csp 3 atoms in the vicinity of the morpholine ring are slightly strained, as indicated by the values of 113.08 (13) and 115.18 (14) for C-C-C angles and 106.98 (13) for the N-C-C angle.