The title compound, C 16 H 27 Cl 3 N 2 O 5 , which is an enantiopure dipeptide trichloroethyl ester, adopts an extended conformation. The molecules are linked via -NHÁ Á ÁO C hydrogen bonds into a unique -spiral assembly along the c axis.
O-Benzyl-N-tert-butoxycarbonyl-l-threonyl-l-proline trichloroethyl ester [Boc-l-Thr(Bzl)-l-Pro-OTce]
✍ Scribed by Oku, Hiroyuki ;Kuriyama, Keisuke ;Omi, Kazuto ;Yamada, Keiichi ;Katakai, Ryoichi
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 458 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
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
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