The asymmetric unit of the title compound, C~22~H~29~N~3~O~5~S, contains two independent molecules, __A__ and __B__, which differ slightly in the orientation of the ethyl and tosyl groups with respect to the attached pyrrolidine ring, as evidenced by the relevant torsion angles. In both molecules, t
4,4,7,7-Tetramethyl-2-tosyl-2,3,3a,4,6,7,8,9-octahydro-1H-pyrrolo[3,4-c]pyrano[6,5-b]cyclohexan-9-one
โ Scribed by Chinnakali, K. ;Sudha, D. ;Jayagopi, M. ;Raghunathan, R. ;Fun, Hoong-Kun
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 835 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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โฆ Synopsis
The title compound, C~22~H~29~NO~4~S, crystallizes with three independent molecules, A, B and C, in the asymmetric unit. Each of the three independent molecules adopts a folded conformation, with the phenylsulfonyl group lying over the pyranocyclohexanone ring system, and with the pyrrolidine and dihydropyran rings cis-fused. In all three molecules, the pyrrolidine ring has a twist conformation and the dihydropyran ring is in a half-chair conformation. The cyclohexenone rings adopt envelope conformations, with the flap atom puckered towards the phenylsulfonyl group in molecule A, and away from that group in molecules B and C, resulting in a different overall conformation for molecule A compared to B and C. In all molecules, the tosyl group is equatorially attached to the pyrrolidine ring. In the crystal structure, the molecules are linked into a three-dimensional framework by CโH...O hydrogen bonds.
๐ SIMILAR VOLUMES
In the title compound, C~20~H~25~N~3~O~5~S, the pyrrolidine ring is __trans__-fused to the dihydropyran ring. The pyrrolidine ring adopts a twist conformation and the dihydropyran ring is in an envelope conformation. The tosyl group is attached to the pyrrolidine ring in a biaxial position and its b
The title compound, C 23 H 25 BrO 3 , was synthesized by the reaction of p-bromobenzaldehyde with dimedone and HClO 4 / SiO 2 in EtOH. In the molecule, the dihydropyran ring adopts a boat conformation and the two cyclohexene rings are in a trans conformation.
The title compound, C 21 H 20 ClN 3 O 2 , was synthesized by the reaction of 4-chlorobenzaldehyde and 3-(5,5-dimethyl-3-oxocyclohex-1-enylamino)propanoic acid with malononitrile in ethylene glycol under microwave irradiation. The dihydropyridine ring has a boat conformation. The pyrimidine ring adop