Cycloadditions of Ketene Diethyl Acetal and 2-Methylene-1,3-dioxepane to Electrophilic Alkenes †
✍ Scribed by Johnston, Keith; Padias, Anne Buyle; Bates, Robert B.; Hall, H. K.
- Book ID
- 126417105
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 83 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0743-7463
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📜 SIMILAR VOLUMES
The stable cyclic ketene acetal, 2-metbylene-1,3-dioxepane, 7, has been polymerized cat ionically in pentane, CHzClj and THF at 25°C to form a polymer which is composed of both ring-opened (40-50% ) and ring-retained (50-60%) structures. Init iatiorr was catalyzed by using H2S0, -supported on activa
## Abstract Cyclic ketene __N,N__‐acetals derived from imidazolidine (4a, c) and 2,3‐dihydrobenzimidazole (6a–c) add methanesulphonyl azide (2a) or picryl azide (2f) to afford the zwitterions 5 and 7, respectively. The structure of 7d is elucidated by X‐ray crystallography. Reversibility of formati