Abstract:
α-Stannyl sulfoxides, 1-(tributylstannyl)-1-(phenylsulfinyl)cyclopropane (1) could undergo the destannylative Pummerer-type rearrangement (the stanna-Pummerer rearrangement) when reacted with tert-butyldimethylchlorosilane in refluxing dichloromethane leading to give a-siloxy cyclopropyl sulfide 3. Similarly, 1(trimethylstannyl)-1-(phenylsulf1nyl)ethene (2) could undergo the same rearrangement on treatment with acyl chlorides in refluxing dichloromethane to afford ketene-O,Sacetals 4 (Scheme I). he α-stannyl sulfones, l-(tributylstannyl)-1(phenylsulfonyl)cyclopropane (5) and 1-(tributylstannyl)-1-(phenylsulfonyl)ethene (6) reacted with acyl chlorides in refluxing toluene to provide the corresponding ketosulfones 7 and 8 (Scheme II)
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