Selenonium ionic liquid as an efficient catalyst for the synthesis of thioacetals under solvent-free conditions
✍ Scribed by Eder J. Lenardão; Elton L. Borges; Samuel R. Mendes; Gelson Perin; Raquel G. Jacob
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 95 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Acidic ionic liquid butyl ethyl phenyl selenonium tetrafluoroborate, [BEPSe]BF 4 , was successfully employed as a catalyst for the synthesis of several dithioacetals in the absence of a solvent. The method is general and selectively afforded thioacetals derived from aldehydes and ketones in good yields.
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