3-[3,5-Dimethoxy-2-(trimethylsilyl)phenyl]-4-trimethylsilylsydnone
✍ Scribed by Grossie, David A. ;Sun, Lihong ;Turnbull, Kenneth
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 244 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 16 H 26 N 2 O 4 Si 2 , is a mesoionic compound of the sydnone class. Its molecular structure reveals the two planar ring fragments mutually twisted by 74.88 (10) . The crystal packing is characterized by a one-dimensional molecular array generated by C-HÁ Á ÁO interactions.
📜 SIMILAR VOLUMES
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
The title compound, C~20~H~17~NO~6~, was synthesized by the reaction of syringaldehyde with hippuric acid. The molecule adopts a __Z__ configuration about the central olefinic bond. The two benzene rings and the oxazolone ring are almost coplanar. The crystal structure is stabilized by weak intermol
## Abstract 3.4‐Dimethoxy‐phenylmagnesiumbromid wurde mit [3.4‐Dimethoxy‐benzal]‐brenztraubensäuremethylester (VIIb) zum 2.4‐Bis‐[3.4‐dimethoxy‐phenyl]‐2‐hydroxy‐buten‐(3)‐säuremethylester (Ib) umgesetzt. Die bei alkalischer Verseifung von Ib entstehende β.γ‐ungesättigte α‐Hydroxysäure ist unbestän