The title compound, C 24 H 19 NO 5 , contains five fused rings, of which three are planar and the other two have twisted and flattened boat forms. The crystal structure is stabilized by intra-and intermolecular N-HÁ Á ÁO, O-HÁ Á ÁO and C-HÁ Á ÁO hydrogen bonds.
1-Oxo-13c-propoxy-1,13c-dihydrodibenzo[a,kl]xanthene
✍ Scribed by Tan, Duan-Min ;Cai, Yue-Peng ;Liao, Miao-Fen ;Su, Cheng-Yong ;Xu, Zun-Le ;Kang, Bei-Sheng
- Publisher
- International Union of Crystallography
- Year
- 2001
- Tongue
- English
- Weight
- 193 KB
- Volume
- 57
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 23 H 18 O 3 , is composed of ®ve rings with one chiral C atom. It crystallizes in the chiral space group P2 1 . with two molecules per asymmetric unit. These molecules are enantiomeric and exhibit normal geometry. The n-propoxy group in one of the pairs is disordered.
📜 SIMILAR VOLUMES
The title compound, C 21 H 16 O 3 , is a key intermediate in the design of chiral amines. It is composed of three benzene rings and two other six-membered rings with a common chiral C atom. Racemic dimers are generated by CÐHÁ Á ÁO hydrogen bonds, formed by phenyl CÐH groups and carbonyl O atoms.
The title compound, C 21 H 14 O 4 , containing three chiral C atoms, is a key intermediate in the design of chiral alcohols. Racemic dimers are generated by C-HÁ Á ÁO hydrogen bonds formed between phenyl C-H groups and epoxy O atoms.
The title compound, C 23 H 24 N 4 , was synthesized from 3,3 0diallyl-1,1 0 -propylenedi(benzimidazole) dibromide and NaH in tetrahydrofuran solution. In the molecule, the diazepine ring exhibits a boat conformation.