93845-39-7Relevant academic research and scientific papers
STANNOUS (II) TRIFLATE PROMOTED REARRANGEMENT OF β-KETO SULFOXIDES. SYNTHESIS OF 1,4-DIKETONES
Shimizu, Makoto,Akiyama, Takahiko,Mukaiyama, Teruaki
, p. 1531 - 1534 (1984)
Stannous triflate promotes rearrangement of β-keto sulfoxides to generate α-thiocarbocation, which in turn react with silyl enol ethers to give 2-arylsulfenyl-1,4-diketones in good yields.
