(3R,3aS,6R,6aR)-tert-Butyl N-(6-chloro-2-oxo-6a-phenylperhydrofuro[3,2-b]furan-3-yl)carbamate
✍ Scribed by Erdsack, Jörg ;Schürmann, Markus ;Preut, Hans ;Krause, Norbert
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 654 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The chiral title compound, C 17 H 20 ClNO 5 , arose as a side product during the synthesis of novel furanomycin derivatives. The stereochemistry at the bicyclic core is consistent with a halolactonization step. The five-membered rings are nearly perpendicular to each other [torsion angle at the common bond: À88.3 (3) ].
📜 SIMILAR VOLUMES
A view of (I), with the atomic numbering scheme. Displacement ellipsoids are drawn at the 30% probability level.
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