Intermolecular N-H•••O and C-H••.bul.O Interactions Form a Two-Dimensional Network in (2S,4S,5R)-(-)-3,4-Dimethyl-5-phenyl-2-(pyrrol-2-yl)-1,3-oxazolidine. -Title compound (I) crystallizes with two molecules in an asymmetric unit. The oxazolidine rings of the two molecules adopt slightly differing
C—H⋯O and C—H⋯π(arene) interactions in (2S,4S,5R)-(–)-2-(4-propoxyphenyl)-3,4-dimethyl-5-phenyl-1,3-oxazolidine
✍ Scribed by Duffy, Marina ;Gallagher, John F. ;Lough, Alan J.
- Publisher
- International Union of Crystallography
- Year
- 2004
- Tongue
- English
- Weight
- 331 KB
- Volume
- 60
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
In the title compound, C 22 H 20 N 2 O 3 , the phenyl substituents adopt equatorial orientations. The seven-membered heterocyclic ring adopts a distorted chair conformation. In the solid state, the symmetry-related molecules are linked by intermolecular CÐHÁ Á ÁO hydrogen bonds to form a supramolecu
The molecules of the title compound, C 26 H 16 FN 3 O, are linked into chains of edge-fused rings by a combination of C-HÁ Á ÁN and C-HÁ Á ÁO hydrogen bonds, and these chains are linked into sheets by a single C-HÁ Á Á(arene) hydrogen bond.