3,7,7a-Tri-epi-casuarine pentaacetate
✍ Scribed by Punzo, Francesco ;Watkin, David J. ;Van Ameijde, Jeroen ;Horne, Graeme ;Fleet, George W. J. ;Wormald, Mark R. ;Nash, Robert J.
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 251 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
The relative stereochemistry at six contiguous centres in an analogue of the natural product casuarine, viz. 3,7,7a-tri-epicasuarine pentaacetate, C 18 H 25 NO 10 , has been established by an analysis of a crystalline pentaacetate.
📜 SIMILAR VOLUMES
Partial Synthesis of Grandidones A, 7‐Epi‐A, B, 7‐Epi‐B, C, D and 7‐Epi‐D, from 14‐Hydroxytaxodione Oxydative addition of coleon U (**6**) to 14‐hydroxytaxodione (**5**) in the presence of __Fétizon__'s reagent mainly leads to grandidone A (**1a**) and 7‐epigrandidone A (**1b**) (__ca.__ 15:1), whe
In the title molecule, C 12 H 10 O 4 , the lactone and benzene rings are coplanar, while the plane of the acetyl substituent is rotated by 12.26 (9) from the molecular plane. The molecules stack throughinteractions along [100] and these stacks are laterally connected by C-HÁ Á ÁO hydrogen bonds alon