5-Benzoyl-1-cyclohexyl-3-(m-nitrophenyl)-2-phenylpyrrolidine-spiro-4,2′-(6′-methoxy-1′-tetralone)
✍ Scribed by Jeyabharathi, A. ;Ponnuswamy, M. N. ;Raj, A. Amal ;Raghunathan, R. ;Fun, Hoong-Kun
- Publisher
- International Union of Crystallography
- Year
- 2002
- Tongue
- English
- Weight
- 225 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
In the title molecule, C 39 H 38 N 2 O 5 , the pyrrolidine ring is in an envelope conformation and the cyclohexyl ring adopts a chair conformation. The cyclohexanone ring in the tetralone moiety adopts a sofa conformation. The molecular packing in the crystal is stabilized by CÐHÁ Á Á% interactions in addition to van der Waals forces.
📜 SIMILAR VOLUMES
The indole moiety of the title compound, C 23 H 24 N 2 O 3 , is planar; but the pyrrolidine ring adopts an envelope conformation. The conformation is stabilized by intramolecular CÐ HÁ Á ÁO interactions and the packing of the molecules is stabilized by strong NÐHÁ Á ÁN hydrogen bonds.
In the title compound, C 26 H 27 NO 3 , the pyrrolidine ring adopts an envelope conformation. The indanedione group is planar, the dihedral angle between the fused five-and six-membered rings of this group being 1.1 (2) . There are intramolecular C-HÁ Á ÁO and C-HÁ Á Á interactions.
In the title compound, C 29 H 26 N 2 O 3 , the pyrrolidine ring adopts an envelope conformation and the cyclohexane ring adopts a chair conformation. The structure is stabilized by intramolecular CÐHÁ Á ÁO and %±% interactions.