85920-92-9Relevant articles and documents
STANNOUS (II) TRIFLATE PROMOTED REARRANGEMENT OF β-KETO SULFOXIDES. SYNTHESIS OF 1,4-DIKETONES
Shimizu, Makoto,Akiyama, Takahiko,Mukaiyama, Teruaki
, p. 1531 - 1534 (2007/10/02)
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.
A REGIOSPECIFIC SYNTHESIS OF γ-KETO ESTERS: THE ALKYLATION OF O-SILYLATED ENOLATES WITH METHYL α-CHLORO-α-PHENYLTHIOACETATE
Lee, Thomas V.,Okonkwo, Jonathan O.
, p. 323 - 326 (2007/10/02)
Methyl α-chloro-α-phenylthio acetate (2) regiospecifically alkylates O-silylated enolates to form γ-keto esters.