(1aS,1bS,4aR,4bR,7aS,10R)-Methyl 1a,1b,4a,4b,7a,8,10,11-octahydro-8-oxo-bis(2-methyl-1,3-oxazino)[6,5,4-cd][4,5,6-de]thiazolo[3,2-a]azepine-10-carboxylate
✍ Scribed by Hörger, Rolf ;Marsch, Michael ;Geyer, Armin ;Harms, Klaus
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 179 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The absolute configuration of the title tetracyclic bis-oxazine, C 14 H 17 N 3 O 5 S, has been determined. It is an unexpected product from the attempt to synthesize a new class of bisoxazolines. The seven-membered lactam ring exhibits four axial (O and N) and one equatorial (S) substituents. The ortho-condensed and cis-configurated oxazine rings are positioned on opposite sides of the lactam ring.
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The title compound, C 27 H 34 ClNO, was synthesized by a direct condensation reaction. The molecule has three chiral centres, which exhibit R, S and R absolute configurations, respectively. Two six-membered rings with different conformations coexist in the structure and they form a trans ring juncti
In the title compound, C 22 H 21 NO 5 , the pyrrolidine ring and the five-membered ring in the indene group have envelope conformations, while the furan ring adopts a twist conformation. Weak intermolecular C-HÁ Á ÁO interactions link the molecules into centrosymmetric dimers. The crystal packing is
The title compound, C 11 H 15 N 3 O 6 S, is a 2 0 ,3 0 -thiazine-fused bicyclic nucleoside. The furanose ring adopts a 3 0 -endo,4 0 -exo conformation 4 T 3 . The orientation of the pyrimidine ring is anti with respect to the sugar group. The crystal packing is stabilized by intermolecular N-HÁ Á ÁO