Chemistry Letters p. 549 - 552 (1983)
Update date:2022-08-03
Takeda, Takeshi
Tsuchida, Toshio
Ando, Kazuo
Fujiwara, Tooru
3-Alkyl-2-cyclobutenones were produced by the sila-Pummerer rearrangement of 1-acetoxy-1-alkyl-3-phenylsulfinyl-3-trimethylsilylcyclobutanes followed by hydrolysis. β-Phenylthio-α,β- and β,γ-unsaturated ketones were major products when the corresponding cyclobutanols were employed.
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