Properties and Reactions of Substituted 1,2-Thiazetidine 1,1-Dioxides: Fluoride Catalyzed Reactions of Silylated β-Sultams with Electrophiles
✍ Scribed by Martin Müller; Hans-Hartwig Otto
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 581 KB
- Volume
- 324
- Category
- Article
- ISSN
- 0365-6233
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📜 SIMILAR VOLUMES
## Abstract 4‐α‐Hydroxyalkylated β‐sultams 1/5 are transformed into 4‐alkylidene‐β‐sultams 4/7 by elimination and desilylation reactions. Another route to an exocyclic double bond in the β‐sultam system has been found to be the Peterson olefination starting from 4 silylated β‐sultams 8, 10, and 11.
## Abstract The introduction of functional groups at the 4‐position of the __β__‐sultam ring was realized by the synthesis of mono‐ and disubstituted derivatives by reactions of __N__‐silylated __β__‐sultams with electrophiles in the presence of BuLi or LDA. As electrophiles, ketones, chlorosilanes