76634-95-2Relevant articles and documents
AN EFFICIENT REGIO AND STEREOSELECTIVE SYNTHESIS OF SILYL ENOL ETHERS
Ahmad, Saeed,Khan, M. Amin,Iqbal, Javed
, p. 1679 - 1684 (2007/10/02)
Ketones and aldehydes on treatment with NaBr-Me3SiCl-Et3N in DMF at ambient temperature yield silyl enol ethers with high regio- and stereoselectivity.
A CONVENIENT PREPARATION METHOD OF THE VINYLIC HALIDE ISOMER OF CHLOROTRIMETHYLSILYL ENOL ETHERS
Poirier, Jean-Marie,Hennequin, Laurent
, p. 217 - 224 (2007/10/02)
Reaction of trimethylsilyliodide (generated in situ from trimethylsilylchloride and sodium iodide) in the presence of triethylamine in acetonitrile with α-chloroketones yields the vinylic halide isomer of chlorotrimethylsilyl enol ethers.
Alkylation and arylation of 2-trimethylsiloxyallyl halides. A new regiospecific route to silyl enol ethers
Sakurai, Hideki,Shirahata, Akihiko,Araki, Yoshitaka,Hosomi, Akira
, p. 2325 - 2328 (2007/10/02)
Alkylation and arylation of 2-trimethylsiloxyallyl halides with lithium dialkyl- and diarylcuprate, respectively, gave silyl enol ethers in a regiospecific manner.