Synthesis of Allyl Aryl Sulfone Derivatives from BaylisHillman Acetates in Water
✍ Scribed by Konkala Karnakar; Jilla Shankar; Sabbavarapu Narayana Murthy; Yadavalli Venkata Durga Nageswar
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- German
- Weight
- 172 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Various phenyl and p‐tolyl allyl sulfone derivatives were prepared stereoselectively by reacting BaylisHillman acetates with sodium 4‐R‐benzenesulfinate (R=H, Me) in H~2~O. The reaction was very efficient in providing the corresponding sulfone derivatives in good to excellent yields (Table).
📜 SIMILAR VOLUMES
Reactions of potassium acetate and the sodium salt of p-toluenesulfinic acid with acetates of Baylis-Hillman adducts produce substituted allyl acetates and allyl sulfones respectively. Ionic liquids are utilized in place of conventional solvents.