(−)-N-(tert-Butoxycarbonyl)-l-proline-2-thioamide (Boc-l-Pro-thioamide)
✍ Scribed by Oku, Hiroyuki ;Yoshinari, Takamasa ;Yamada, Keiichi ;Katakai, Ryoichi
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 234 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Crystals of the title compound, C 10 H 18 N 2 O 2 S, which is an enantiopure N-protected l-prolinethioamide, were successfully grown from a tetrahydrofuran solution. Intermolecular N-HÁ Á ÁO hydrogen bonds are observed between thioamide -NH 2 and Boc-carbonyl C O groups, but the thioamide C S group is not involved in hydrogen bonding.
📜 SIMILAR VOLUMES
Single-crystal X-ray study T = 173 K Mean '(C±C) = 0.010 A Ê R factor = 0.058 wR factor = 0.116 Data-to-parameter ratio = 9.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The crystal structure of the title compound, C 16 H 30 N 2 O 5 , has been determined. In the asymmetric unit, there are three independent molecules which adopt extended -sheet conformations. These molecules are linked together into an in®nite column by six hydrogen bonds of the type ±NHÁ Á ÁO C. All
Crystals of the title compound, C 17 H 30 N 2 O 7 , were successfully grown from ethyl acetate at room temperature. In the crystal structure, a free carboxylic acid group is found at the terminal C atom. The free acid ÐOH group contributes to a hydrogenbond network, together with two NÐHÁ Á ÁO inter