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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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