In the crystals of the title compound, C 19 H 24 O 8 , the molecules adopt a conformation in which the bulky 2,6-dimethoxyphenoxy and 4-hydroxy-3,5-dimethoxyphenyl groups are distant from each other. The O(phenoxy)ÐCÐCÐC(phenyl) torsion angle between these groups is À177.27 (10) . The conformation i
erythro-2-(2,6-Dimethoxy-4-methylphenoxy)-1-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,3-diol
✍ Scribed by Langer, Vratislav ;Lundquist, Knut ;Miksche, Gerhard E.
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 196 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.001 A Ê R factor = 0.044 wR factor = 0.124 Data-to-parameter ratio = 25.9 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.003 A Ê R factor = 0.051 wR factor = 0.123 Data-to-parameter ratio = 12.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
Single-crystal X-ray study T = 183 K Mean '(C±C) = 0.002 A Ê Disorder in main residue R factor = 0.049 wR factor = 0.144 Data-to-parameter ratio = 16.2 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
The title compound, C 26 H 30 O 7 , was obtained by the Grignard reaction of one molecule of 4-methoxybenzylmagnesium chloride with two molecules of 3,5-dimethoxybenzaldehyde. The two new chiral centers have the same absolute con®guration R (S), and the two hydroxyl groups, surrounded by the three b