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.
13c-Methoxy-1,2,3,13c-tetrahydrodibenzo[a,kl]xanthan-1-one
✍ Scribed by Pang, Ji-Yan ;Cai, Jiwen ;Tan, Duan-Ming ;Chen, Zhi-Peng ;Xu, Zun-Le
- Publisher
- International Union of Crystallography
- Year
- 2002
- Tongue
- English
- Weight
- 317 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
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.
📜 SIMILAR VOLUMES
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.
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.
Single-crystal X-ray study T = 295 K Mean '(C±C) = 0.004 A Ê R factor = 0.052 wR factor = 0.113 Data-to-parameter ratio = 7.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
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.