The crystal structure of the title compound, C~36~H~40~N~2~O~2~, has been determined at 173 (2) K. The molecule has __C__ ~2~ symmetry and the asymmetric unit contains one half-molecule. An intramolecular O—H...N hydrogen bond is formed between the phenol OH group and the Schiff base N atom.
1-tert-Butyl 2-methyl 4-(R)-hydroxypyrrolidine-1,2-(2S)-dicarboxylate
✍ Scribed by Clegg, William ;Deboves, Hervé J. C. ;Elsegood, Mark R. J.
- Publisher
- International Union of Crystallography
- Year
- 2003
- Tongue
- English
- Weight
- 265 KB
- Volume
- 59
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The centrosymmetric title compound, C 54 H 70 O 4 , contains a benzene ring at the centre and four 2-tert-butyl-4-methylphenoxymethyl substituents. In the structure of the molecule, some of the benzene rings are coplanar. The title compound displays intramolecular CÐHÁ Á ÁO hydrogen bonds. The cryst
The title compound, C 27 H 39 N 3 O 9 , is a key intermediate in the synthesis of novel -turn mimetics based on electrophilic amination of enantiomerically pure (S)-pyroglutamic acid. The molecule adopts an extended conformation which is not stabilized by either intra-or intermolecular hydrogen bond
In the molecule of the title compound, C~28~H~42~O~2~, the two cyclohexane rings adopt chair conformations. The olefinic bond and carbonyl group are approximately coplanar.