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 comm
✦ LIBER ✦
rac-N-(6a-Butyl-6-chloro-2-oxoperhydrofuro[3,2-b]furan-3-yl)-2,2,2-trifluoroacetamide
✍ Scribed by Erdsack, Jörg ;Schürmann, Markus ;Preut, Hans ;Krause, Norbert
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 518 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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