A view of (I), with the atomic numbering scheme. Displacement ellipsoids are drawn at the 30% probability level.
(6aR)-1-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-(methylcarbonyloxy)perhydro-4-picenylmethyl acetate
✍ Scribed by Flekhter, Oxana B. ;Medvedeva, Natalya I. ;Suponitsky, Kyrill Yu.
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 250 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
No coin nor oath required. For personal study only.
✦ Synopsis
The title compound, C 34 H 56 O 5 , an oleanane triterpene, is a key intermediate in the synthetic route from betulin to 18(19)oleanene triterpenoids. In the molecule, all bond lengths and angles are normal. The hydroxy groups are involved in intermolecular O-HÁ Á ÁO hydrogen bonds, which link the molecules into zigzag chains running along the a axis. The crystal packing is further stabilized by weak intermolecular C-HÁ Á ÁO hydrogen bonds.
📜 SIMILAR VOLUMES
## Abstract Aus Harnstoff und 2 Mol α.α′‐Dichlor‐diisobutyläther (**1**) entsteht 4‐Hydroxy‐2.8‐diisopropyl‐3.3.9.9‐tetramethyl‐perhydropyrimido[4.3‐__b__][1.3]oxazin‐6‐on (**3**). Dieses läßt sich zu dem sehr stabilen Heterocyclus **6** hydrieren. Die Struktur von **3** wird durch Abbau zu **7**‐*
The title compound, C 21 H 20 ClN 3 O 2 , was synthesized by the reaction of 4-chlorobenzaldehyde and 3-(5,5-dimethyl-3-oxocyclohex-1-enylamino)propanoic acid with malononitrile in ethylene glycol under microwave irradiation. The dihydropyridine ring has a boat conformation. The pyrimidine ring adop
In the title compound, C 19 H 15 Cl 4 NO 3 , the isoindole unit is planar and the oxazino ring adopts a twist-boat conformation. The dihedral angle between the isoindole unit and the phenyl ring is 50.46 (13) . The molecules are linked via intermolecular O-HÁ Á ÁO hydrogen bonds and weak C-HÁ Á ÁO a